Hv1 modulators and uses

ABSTRACT

The present invention provides novel agents for modulation of Hv1 channels. The present invention provides agents for activating and/or inhibiting Hv1 channel function and/or activity, and reagents and methods relating thereto.

RELATED APPLICATIONS

This application is a continuation of U.S. patent application Ser. No. 16/474,906, filed Jun. 28, 2019, now pending, which is a National Phase Patent Application claiming benefit of priority under 35 U.S.C. § 371 to International (PCT) Patent Application serial number PCT/US2017/068896, filed Dec. 29, 2017, now expired, which claims benefit to U.S. Provisional Application No. 62/441,097, filed Dec. 30, 2016, now expired and U.S. Provisional Application No. 62/447,433, filed Jan. 17, 2017, now expired. The aforementioned applications are expressly incorporated herein by reference in their entirety and for all purposes.

ACKNOWLEDGEMENT OF FEDERAL RESEARCH SUPPORT

One or more aspects or features of an invention described in the present disclosure may have been made with government support under contract number RO1GM111716 awarded by the National Institutes of Health. The United States Government may have certain rights in such invention(s).

BACKGROUND

Voltage-gated ion channels facilitate the transfer of ions across cell membranes and function as key components of essential cellular processes. One particular type of voltage-gated ion channel is the voltage-gated proton channel (Hv1). Hv1 is a transmembrane protein that regulates the transfer of protons across cell membranes. When the Hv1 channel is open, protons permeate the channel and cross the cellular membrane.

The Hv1 channel is expressed in many different tissues and is associated with a wide variety of physiological and pathological processes. For example, Hv1 channels may play a role in immune defense, sperm activity, and cancer progression. For these and other reasons, Hv1 may be an attractive drug target (Seredenina, T., et al. “Voltage-gated proton channels as novel drug targets: from NADPH oxidase regulation to sperm biology.” Antioxid Redox Signal. 10; 23(5): 490-513 (2015)). However, clinically compatible Hv1 activators or inhibitors are not known. For these reasons, there is a need for the development of activators and inhibitors of Hv1 channels.

SUMMARY

The present disclosure provides technologies relating to modulation of Hv1 channels. Among other things, the present disclosure provides Hv1 modulating agents, and various compositions and methods relating thereto.

In some embodiments, an Hv1 modulating agent is or comprises an engineered polypeptide component having an inhibitor cysteine knot (ICK)-like structural motif.

In some embodiments, an Hv1 modulating agent is or comprises an engineered polypeptide component that includes one or more toxin sequence elements, each of which has an amino acid sequence that is substantially identical to, but differs from, that of a corresponding element found in a wild-type toxin.

In some embodiments, an Hv1 modulating agent shares one or more cysteines with a wild-type toxin sequence. In some embodiments, an Hv1 modulating agent shares the same approximate relative position of cysteines with a wild-type toxin.

In some embodiments, an Hv1 modulating agent is or comprises a polypeptide sequence set forth in Tables 2A, 3A, and 4.

In some embodiments, an Hv1 modulating agent is encoded by a nucleotide sequence that is or comprises a sequence set forth in Tables 2C and 3B.

In some embodiments, an Hv1 modulating agent can be expressed from a vector including a nucleic acid sequence encoding the Hv1 modulating agent.

In some embodiments, an Hv1 modulating agent binds to the external surface of human Hv1. In some embodiments, an Hv1 modulating agent binds to the S3-S4 external loop region of human Hv1.

In some embodiments, an Hv1 modulating agent inhibits human Hv1 function. For example, in some embodiments, an Hv1 modulating agent may decrease or block proton current. In some embodiments, an Hv1 modulating agent may reduce the number or likelihood of Hv1 channel opening. In some embodiments, an Hv1 modulating agent may increase the rate of Hv1 channel closing.

In some embodiments, an Hv1 modulating agent activates human Hv1 function. For example, in some embodiments, an Hv1 modulating agent increases proton current. In some embodiments, an Hv1 modulating agent increase the rate of Hv1 channel opening. In some embodiments, an Hv1 modulating agent slows the rate of Hv1 channel closing.

In some embodiments, an Hv1 modulating agent inhibits sperm capacitation.

In some embodiments, an Hv1 modulating agent decreases reactive oxygen species (ROS) production in white blood cells.

The present invention further provides various reagents and methods associated with Hv1 modulating agents including, for example, systems for identifying and characterizing them, strategies for preparing them, and various therapeutic compositions and methods relating to them. Further description of certain embodiments of these aspects, and others, of the present invention, is presented below.

BRIEF DESCRIPTION OF THE DRAWING

FIG. 1 Presents an amino acid sequence alignment of exemplary Hv1 modulating agents C5 and C6. Six conserved cysteine residues and three disulfide bridges of an inhibitor cysteine knot (ICK)-like structural motif are indicated.

FIG. 2 Presents the amino acid sequences of exemplary Hv1 modulating agents C5 and C6 and the amino acid sequence of hanatoxin (HaTx1). Sequence elements corresponding to sequences in Table 3A are labeled. Conserved cysteine residues are highlighted. NT, N-terminus. CT, C-terminus.

FIG. 3A-F Presents exemplary T-toxin amino acid sequences and effects of T-toxins on hHv1 function. (FIG. 3A) depicts an exemplary T-toxin comprising the amino acid sequence of Hv1 modulating agent C6 linked to a trypsin secretory signal sequence at the N-terminus, a 16 amino acid linker with embedded C-Myc epitope tag at the C-terminus, and a hydrophobic sequence for GPI attachment from the mammalian Lynx1 peptide. (FIG. 3B) depicts an exemplary T-toxin comprising an N-terminal trypsin secretory signal sequence, the amino acid sequence of HaTx1 linked by a flexible 7 amino acid linker to C6, a C-Myc epitope embedded into a 6 amino acid linker at the C-terminus, and a hydrophobic sequence for GPI attachment. (FIG. 3C) depicts an exemplary T-toxin comprising an N-terminal trypsin secretory signal sequence, C6 dimers linked by a rigid 10 amino acid linker, a C-Myc epitope embedded into a 6 amino acid linker at the C-terminus, and a hydrophobic sequence for GPI attachment. (FIG. 3D) depicts an exemplary T-toxin comprising an N-terminal trypsin secretory signal sequence, C6 dimers linked by a flexible 10 amino acid linker, a C-Myc epitope embedded into a 6 amino acid linker at the C-terminus, and a hydrophobic sequence for GPI attachment. (FIG. 3E) depicts an exemplary T-toxin comprising an N-terminal trypsin secretory signal sequence, C6 dimers linked by long flexible 38 amino acid linker, a C-Myc epitope embedded into a 6 amino acid linker at the C-terminus, and a hydrophobic sequence for GPI attachment. (FIG. 3F) shows inhibition of wild-type hHv1 measured as unblocked fractional current in oocytes expressing only hHv1 or both hHv1 and T-toxin.

FIG. 4A-B Illustrates activating and inhibiting effects of exemplary Hv1 modulators C5 and C6 on hHv1. Whole-cell patch clamp recordings were performed on HEK-293T cells over-expressing hHv1. Proton currents are shown with C5 (FIG. 4A) and C6 (FIG. 4B) versus current without any peptide or modifications (black traces).

FIG. 5A-K Illustrates that Hv1 modulating agent C6 affects response of sperm to progesterone, but not other changes related to sperm capacitation. C6 did not affect the vitality (FIG. 5A), the protein tyrosine phosphorylation (FIG. 5F and FIG. 5G), or the cholesterol content of the membranes (FIG. 5H). C6 did not significantly alter the mobility of sperm (FIGS. 5B-5E). C6 did affect the response of sperm to progesterone. The increase of cytosolic calcium triggered by progesterone is diminished in the presence of the Hv1 modulating agent and the acrosome reaction induced by the hormone is inhibited (FIGS. 5I-5K). All responses with C6 were compared to control peptide. VSL, velocity straight line; PROG, progression; VAP, velocity average path; Capac, capacitating medium (Human tubal fluid (HTF) media supplemented with 5 mg/mL BSA; as described, for example, in Pocognoni, C. A., et al., “PerfringolysinO as a useful tool to study human sperm physiology,” Fertility & Sterility 99(1): 99-106(2013)).

FIG. 6A-B Demonstrates that Hv1 modulating agent C6 blocks production of ROS in human blood cells in a dose-dependent manner. Phorbol myristate acetate (PMA) was used to stimulate ROS production as shown by the increase of fluorescence over baseline (blood). The known inhibitor of Hv1, zinc (Zn), blocks to background levels. Various concentrations of C6 also blocked fluorescence intensity in a dose-dependent manner. Two other toxins that block potassium channels with nM affinity (Moka and KTX) had no effect. FIG. 6A shows relative fluorescence intensity, measured at 590 nM (excited at 530 nM) using Amplex Red, which reacts with ROS to give a fluorescent product, for whole blood alone, PMA-stimulated whole blood, and PMA-stimulated whole blood with various inhibitors. 10 μM of MOKA toxin was used as a control. FIG. 6B shows dose response curve plotted as the percentage of fluorescence from PMA-stimulated whole blood blocked versus concentration of C6 present. MOKA toxin and KTX were used as controls and showed no effect at 10 μM.

FIG. 7A-B Presents an exemplary T-toxin nucleotide (FIG. 7A; SEQ ID NO: 807) and amino acid (FIG. 7B; SEQ ID NO: 808) sequence comprising a PDGFR transmembrane helix which links an internal mVenus fluorescent protein to an external C6.

FIG. 8A-G Illustrates effects of Hv1 modulating agent C6 tethered to HEK-293T cell surfaces via a PDGFR transmembrane link. (FIG. 8A) shows current recordings for WT Hv1 without any tether or peptide (top), expressed with the transmembrane mVenus without a peptide sequence (middle), or expressed with tethered mVenus-C6 (bottom). (FIG. 8B) shows WT Hv1 current with various amounts of tethered toxin plasmid normalized to current with the transmembrane tether without peptide (I(C6)/I(notox)) or to WT Hv1 with no tether expressed (I(C6)/I(Hv1)). (FIG. 8C) demonstrates small shifts observed in g-V normalized to the maximum seen for each condition. Black line is WT Hv1, Green line is WT Hv1 with transmembrane without tether, Red line is WT-Hv1 with tethered C6. (FIG. 8D) demonstrates current-voltage (I-V) showing the decrease in current in WT (black), WT with tether without toxin (green) or WT with tethered C6 (red). (FIG. 8E) shows amount of current blocked by 1 μg of expressed tethered C6 in peak (end of pulse) or tail current. Current is normalized to the maximum of either WT alone (I(C6)/I(Hv1)) or the WT co-expressed with a tether without toxin (I(C6)/I(notox)). (FIG. 8F) shows FRET measurements between Hv1-TFP and mVenus transmembrane without toxin or with C6. Normalized fluorescence versus time is fit with a single exponential decay to determine the time constants for fluorescence decay with or without toxin. (FIG. 8G) shows average taus measured with the tether without toxin and with the tether with C6 from the fit in FIG. 8F. Increase in decay rate indicates FRET and indicates an interaction between C6 and Hv1.

FIG. 9A-C Demonstrates that Hv1 modulating agent C6 targets an S3-S4 external loop region of hHv1. (FIG. 9A) illustrates sequence alignments of Ciona intestinalis Hv1 (CiHv1, yellow), human Hv1 (hHv1, cyan), a chimeric Hv1 where an S3-S4 external loop region from hHv1 replaces a corresponding region from CiHv1 (hS3S4CiHv1), a chimeric Hv1 where an S3-S4 external loop region from CiHv1 replaces an hHv1 loop region, as well as three different loop lengths transferred (ShortN, ShortNC, shortC). If C6 blocks (YES) or does not (NO) block the channel is indicated. X indicates that proton currents were not measurable. (FIG. 9B) demonstrates a representative trace (left) for CiHv1 with 1 μM C6 (red trace) or without (black trace), a representative trace (middle) for hS3S4CiHv1 which is sensitive to C6 (red trace, 1 μM C6), and a representative trace (right) for CiS3S4hHv1 which is insensitive to C6 (red trace, 1 μM C6). Black traces are current without any applied peptide. (FIG. 9C) demonstrates results from a cysteine scan of part of the transferred epitope. Bars are the amount of current with 1 μM C6 normalized to current without toxin (Itox/Ictr). Many residues show decreased affinity but only G199 and E192 show dramatically different effects to the WT (first bar).

DEFINITIONS

Component: The term “component” as used herein refers to a relevant part, portion, or moiety of an entity of interest. For example, in some embodiments, an entity of interest may be a polypeptide component.

Comprising: A composition or method described herein as “comprising” one or more named elements or steps is open-ended, meaning that the named elements or steps are essential, but other elements or steps may be added within the scope of the composition or method. To avoid prolixity, it is also understood that any composition or method described as “comprising” (or which “comprises”) one or more named elements or steps also describes the corresponding, more limited composition or method “consisting essentially of” (or which “consists essentially of”) the same named elements or steps, meaning that the composition or method includes the named essential elements or steps and may also include additional elements or steps that do not materially affect the basic and novel characteristic(s) of the composition or method. It is also understood that any composition or method described herein as “comprising” or “consisting essentially of” one or more named elements or steps also describes the corresponding, more limited, and closed-ended composition or method “consisting of” (or “consists of”) the named elements or steps to the exclusion of any other unnamed element or step. In any composition or method disclosed herein, known or disclosed equivalents of any named essential element or step may be substituted for that element or step.

Corresponding to: As used herein, the term “corresponding to” designates the position/identity of a structural element in a compound or composition through comparison with an appropriate reference compound or composition. For example, in some embodiments, a monomeric residue in a polymer (e.g., an amino acid residue in a polypeptide or a nucleic acid residue in a polynucleotide) may be identified as “corresponding to” a residue in an appropriate reference polymer. For example, those of ordinary skill will appreciate that, for purposes of simplicity, residues in a polypeptide are often designated using a canonical numbering system based on a reference related polypeptide, so that an amino acid “corresponding to” a residue at position 190, for example, need not actually be the 190^(th) amino acid in a particular amino acid chain but rather corresponds to the residue found at 190 in the reference polypeptide; those of ordinary skill in the art readily appreciate how to identify “corresponding” amino acids.

Engineered: In general, the term “engineered” refers to the aspect of having been manipulated by the hand of man. For example, a polynucleotide is considered to be “engineered” when two or more sequences, that are not linked together in that order in nature, are manipulated by the hand of man to be directly linked to one another in the engineered polynucleotide. For example, in some embodiments of the present invention, an engineered polynucleotide comprises a regulatory sequence that is found in nature in operative association with a first coding sequence but not in operative association with a second coding sequence, is linked by the hand of man so that it is operatively associated with the second coding sequence. Comparably, a cell or organism is considered to be “engineered” if it has been manipulated so that its genetic information is altered (e.g., new genetic material not previously present has been introduced, for example by transformation, mating, somatic hybridization, transfection, transduction, or other mechanism, or previously present genetic material is altered or removed, for example by substitution or deletion mutation, or by mating protocols). As is common practice and is understood by those in the art, progeny of an engineered polynucleotide or cell are typically still referred to as “engineered” even though the actual manipulation was performed on a prior entity.

Inhibitor Cysteine Knot (ICK)-like structural motif: As used herein, the term “inhibitor cysteine knot (ICK)-like structural motif” designates a peptide structure that has substantial structural similarity to an ICK structural motif. In some embodiments, an ICK-like structural motif has three disulfide bridges. In some embodiments, an ICK-like structural motif has two, one, or zero disulfide bridges. In some embodiments, an ICK-like structural motif has three beta strands. In some embodiments, an ICK-like structural motif has two, one, or zero beta strands. In some embodiments, an ICK-like structural motif has an amino acid sequence with six conserved cysteine residues of an ICK structural motif. In some embodiments, an ICK-like structural motif has an amino acid sequence with 5, 4, 3, 2, 1, or 0 conserved cysteine residues of an ICK structural motif.

Hv1 associated disease or condition: As used herein, the phrase “Hv1 associated disease or condition” refers to a disease, disorder, or condition in which cells exhibit relatively abnormal, uncontrolled, or undesired Hv1 channel function. Abnormal or uncontrolled Hv1 function may arise from, among other mechanisms, dysregulatd phosphorylation, differential isoform expression, or single nucleotide polymorphisms (SNPs) that alter Hv1 properties. In some embodiments, abnormal or uncontrolled Hv1 function includes abnormal activation or opening of Hv1 channels. In some embodiments, abnormal or uncontrolled Hv1 function includes abnormal closing of Hv1 channels. In some embodiments, cells that exhibit abnormal or uncontrolled Hv1 function display an abnormal level or regulation of transmembrane proton flux, transmembrane voltage and/or transmembrane pH gradient (ΔpH, defined as pH_(o)-pH_(i)). In some embodiments, such cells display an abnormal level or regulation of NOX enzyme activity and/or reactive oxygen species (ROS) production. A variety of types of Hv1 associated diseases or conditions may exist, for example, inflammation, autoimmunity, cancer, asthma, brain damage in ischemic stroke, Alzheimer's disease, infertility, and numerous other conditions. In some embodiments, an Hv1 associated disease or condition refers to a condition in which Hv1 channel function is within normal, but undesired range. For example, an Hv1 associated disease or condition may refer to a condition in which changing Hv1 function would achieve a more preferred physiological outcome than not changing Hv1 function. For example, suppression of Hv1 function in human sperm may be used as a form of birth control to block fertilization.

Library: As used herein, the term “library” refers to a collection of members. A library may be comprised of any type of members. For example, in some embodiments, a library comprises a collection of phage particles. In some embodiments, a library comprises a collection of peptides. In some embodiments, a library comprises a collection of cells. A library typically includes diverse members (i.e., members of a library differ from each other by virtue of variability in an element, such as a peptide sequence, between members). For example, a library of phage particles can include phage particles that express unique peptides. A library of peptides can include peptides having diverse sequences. A library can include, for example, at least 10¹, 10², 10³, 10⁴, 10⁵, 10⁶, 10⁷, 10⁸, 10⁹, or more unique members.

Modulate: The term “modulate” is used to refer to the characteristic of changing the state and/or nature of an entity of interest. For example, a particular agent is considered to modulate an entity of interest if the presence, level, and/or form of the agent correlates with a change in the presence, level, and/or form of the entity of interest. In some embodiments, to modulate means to increase activity. In some embodiments, to modulate means to antagonize, inhibit, or reduce activity. In some embodiments, modulation involves binding or direct interaction between a modulator and the entity of interest. In some embodiments, to modulate means to affect level of a target entity of interest; alternatively or additionally, in some embodiments, to modulate means to affect activity of a target entity without affecting level of the target entity. In some embodiments, to modulate means to affect both level and activity of a target entity of interest. In some embodiments, effects of a modulator are apparent at the level of the whole-cell, tissue, system (e.g. immune system), or whole organism.

Pharmaceutical Composition: As used herein, the term “pharmaceutical composition” refers to a composition that is suitable for administration to a human or animal subject. In some embodiments, a pharmaceutical composition comprises an active agent formulated together with one or more pharmaceutically acceptable carriers. In some embodiments, the active agent is present in a unit dose amount appropriate for administration in a therapeutic regimen. In some embodiments, a therapeutic regimen comprises one or more doses administered according to a schedule that has been determined to show a statistically significant probability of achieving a desired therapeutic effect when administered to a subject or population in need thereof. In some embodiments, a pharmaceutical composition may be specially formulated for administration in solid or liquid form, including those adapted for the following: oral administration, for example, drenches (aqueous or non-aqueous solutions or suspensions), tablets, e.g., those targeted for buccal, sublingual, and systemic absorption, boluses, powders, granules, pastes for application to the tongue; parenteral administration, for example, by subcutaneous, intramuscular, intravenous or epidural injection as, for example, a sterile solution or suspension, or sustained-release formulation; topical application, for example, as a cream, ointment, or a controlled-release patch or spray applied to the skin, lungs, or oral cavity; intravaginally or intrarectally, for example, as a pessary, cream, or foam; sublingually; ocularly; transdermally; or nasally, pulmonary, and to other mucosal surfaces. In some embodiments, a pharmaceutical composition is intended and suitable for administration to a human subject. In some embodiments, a pharmaceutical composition is sterile and substantially pyrogen-free.

Polypeptide: As used herein, the term “polypeptide” refers to any polymeric chain of amino acids. In some embodiments, a polypeptide has an amino acid sequence that occurs in nature. In some embodiments, a polypeptide has an amino acid sequence that does not occur in nature. In some embodiments, a polypeptide has an amino acid sequence that is engineered in that it is designed and/or produced through action of the hand of man. In some embodiments, a polypeptide may comprise or consist of natural amino acids, non-natural amino acids, or both. In some embodiments, a polypeptide may comprise or consist of only natural amino acids or only non-natural amino acids. In some embodiments, a polypeptide may comprise D-amino acids, L-amino acids, or both. In some embodiments, a polypeptide may comprise only D-amino acids. In some embodiments, a polypeptide may comprise only L-amino acids. In some embodiments, a polypeptide is referred to as a “peptide.”

Substantial identity: As used herein, the term “substantial identity” refers to a comparison between amino acid or nucleic acid sequences. As will be appreciated by those of ordinary skill in the art, two sequences are generally considered to be “substantially identical” if they contain identical residues in corresponding positions. As is well known in this art, amino acid or nucleic acid sequences may be compared using any of a variety of algorithms, including those available in commercial computer programs such as BLASTN for nucleotide sequences and BLASTP, gapped BLAST, and PSI-BLAST for amino acid sequences. Exemplary such programs are described in Altschul et al., Basic local alignment search tool, J. Mol. Biol., 215(3): 403-410, 1990; Altschul et al., Methods in Enzymology; Altschul et al., Nucleic Acids Res. 25:3389-3402, 1997; Baxevanis et al., Bioinformatics: A Practical Guide to the Analysis of Genes and Proteins, Wiley, 1998; and Misener, et al, (eds.), Bioinformatics Methods and Protocols (Methods in Molecular Biology, Vol. 132), Humana Press, 1999. In addition to identifying identical sequences, the programs mentioned above typically provide an indication of the degree of identity. In some embodiments, two sequences are considered to be substantially identical if at least 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more of their corresponding residues are identical over a relevant stretch of residues. In some embodiments, the relevant stretch is a complete sequence. In some embodiments, the relevant stretch is at least 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 125, 150, 175, 200, 225, 250, 275, 300, 325, 350, 375, 400, 425, 450, 475, 500 or more residues.

Substantial structural similarity: As used herein, the term “substantial structural similarity” refers to presence of shared structural features such as presence and/or identity of particular amino acids at particular positions. In some embodiments the term “substantial structural similarity” refers to presence and/or identity of structural elements (for example: loops, sheets, helices, H-bond donors, H-bond acceptors, glycosylation patterns, salt bridges, and disulfide bonds). In some embodiments, the term “substantial structural similarity” refers to three dimensional arrangement and/or orientation of atoms or moieties relative to one another (for example: distance and/or angles between or among them between an agent of interest and a reference agent).

Toxin: As used herein, the term “toxin” refers to all peptides and/or proteins, of any amino acid length and sequence, in either monomeric or multimeric forms, naturally present in animal venoms or poisons and their non-venom homologues. Non-venom homologues include any molecule present outside of a venom gland or not used as a venom component but similar in sequence, structure and/or function to toxins. Animal toxins include all molecules identified or inferred by any means (e.g., physical, chemical, biochemical, genetic, genomic, proteomic) from animal venoms or poisons, including but not limited to isolation from crude venoms, isolation from venom gland tissues or extracts, identification based on venom gland proteome/proteomics, venome/venomics, transcriptome, and/or EST analysis. In some embodiments, a toxin is a toxin from a venom or poison of a centipede, lizard, scorpion, sea anemone, snail, snake, spider, or toad. In some embodiments, the amino acid sequence of a toxin can be a sequence that encodes an expressed and/or active toxin, or a sequence showing substantial identity thereto. In some embodiments, the amino acid sequence of a toxin is substantially identical to that of a wild-type toxin. In some embodiments, the amino acid sequence of a toxin is less than 100, 90, 80, 70, 60, 50, 40, 30, 20 or fewer amino acids long. In some embodiments, the amino acid sequence of a toxin is more than 5, 6, 7, 8 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30 or more amino acids long. Representative toxins, and their amino acid sequences and source designations are presented in Table 1.

Toxin Sequence Element: The phrase “toxin sequence element” is used herein to refer to a stretch of amino acid sequence, typically at least 5 amino acids in length, that corresponds to an element found in a wild-type toxin. In some embodiments, a toxin sequence element has a length within a range of about 5 to about 100 amino acids. In some embodiments, a toxin sequence has a length of about 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, or more amino acids. In some embodiments, a toxin sequence element has a length within a range of about 5 to about 25 amino acids. In some embodiments, a toxin sequence element differs from a corresponding sequence element found in the wild-type toxin; for example, in some embodiments, a toxin sequence element differs from its corresponding wild-type sequence element, by a sequence variation that includes an addition, substitution, or deletion of at least one amino acid residue. In some embodiments, the variation alters (e.g., adds, substitutes or deletes) 1, 2, 3, 4, 5 or more residues. In some embodiments, the variation alters exactly 1 residue. In some embodiments, the variation alters exactly 2 residues. In some embodiments, the variation alters exactly 3 residues. In some embodiments, the variation alters not more than 5, 4, 3, 2, or 1 residues. In some embodiments, the variation alters fewer than 15%, 14%, 13%, 12%, 11%, 10%, 9%, 8%, 7%, 6%, 5%, 4%, 3%, 2%, or 1% of the relevant residues. In some embodiments, a toxin sequence element corresponds to a full-length toxin. In some embodiments, a toxin sequence element corresponds to a full-length reference wild-type toxin. In some embodiments, a toxin sequence element corresponds to a portion of a reference wild-type toxin. In some embodiments, a toxin sequence element corresponds to a portion of a wild-type reference toxin, which portion is bounded on at least one end by a cysteine residue (e.g., a cysteine residue that, in the wild-type toxin, may participate in a disulfide bond).

Wild-type: As used herein, the term “wild-type” refers to a form of an entity (e.g., a polypeptide or nucleic acid) that has a structure and/or activity as found in nature in a “normal” (as contrasted with mutant, diseased, altered) state or context. In some embodiments, more than one “wild type” form of a particular polypeptide or nucleic acid may exist in nature, for example as “alleles” of a particular gene or normal variants of a particular polypeptide. In some embodiments, that form (or those forms) of a particular polypeptide or nucleic acid that is most commonly observed in a population (e.g., in a human population) is the “wild-type” form.

DETAILED DESCRIPTION OF CERTAIN EMBODIMENTS Hv1 Channel

The voltage-gated proton channel (Hv1), also known as the hydrogen voltage-gated channel 1 (HVCN1), is a protein that in humans is encoded by the HVCN1 gene. There are at least ten species with functionally confirmed Hv1 genes, including human (hHv1) and mouse (mHv1), in addition to several species with predicted Hv1 genes that have not yet been confirmed by expression and electrophysiology studies. Among its functions, Hv1 transports protons (H⁺) across cell membranes (DeCoursey, T. E. “The voltage-gated proton channel: a riddle, wrapped in a mystery, inside an enigma.” Biochemistry 54(21): 3250-68 (2015)). In humans, the Hv1 protein is expressed in a variety of tissues and body systems, including the immune system, the circulatory system, and the reproductive system. In these and other areas, Hv1 plays important physiological functions, such as regulation of cell charge and pH. In the present disclosure the terms Hv1 channel and Hv1 are equivalent.

Hv1 belongs to a superfamily of voltage-gated ion channels. Similar to other voltage-gated ion channels, Hv1 is a transmembrane protein that facilitates the transfer of ions (e.g. H⁺) across cell membranes. Also like other voltage-gated ion channels, Hv1 has a voltage sensor domain (VSD). However, Hv1 channels also have several unique features that distinguish them from other voltage-gated ion channels. For example, Hv1 channels are exquisitely selective for protons, whereas other ion channels such as potassium channels have some permeability to other ions besides K.

According to the National Center for Biotechnology Information (NCBI) Gene database, there are three transcript variants for human HVCN1. Variant 1 (NM 001040107.1) represents the longest transcript. Variant 2 (NM_032369.3) differs in the 5′ untranslated region (UTR) compared to variant 1. Variants 1 and 2 encode the same protein (isoform 1), which is 273 amino acids. Variant 3 (NM_001256413.1) differs in the 5′ UTR, lacks a portion of the 5′ coding region, and initiates translation at a downstream start codon compared with variant 1. The resulting protein (isoform 2) is shorter (253 amino acids) and has a distinct N-terminus compared to isoform 1. The longer isoform (isoform 1) is considered to be most widely expressed, while the shorter isoform (isoform 2) has been found only in B-lymphocytes and exhibits functionally important differences compared to the full-length protein. Recently, another Hv1 isoform (Hv1Sper, post-translationally cleaved) was reported in human sperm. At least seven validated, nonsynonymous single-nucleotide polymorphisms (SNPs) for human HVCN1 have been identified. Only two of these seven have a frequencies above 1%.

Hv1 Channel Structure

The structure of the Hv1 channel differs from other voltage-gated ion channels. Other voltage-gated ion channels consist of six transmembrane segments, with segments S1-S4 constituting the VSD that detects changes in membrane potential and S5-S6 forming the pore domain responsible for selective ion permeation. In contrast, Hv1 channels lack the pore domain (S5-S6). Instead, Hv1 channels have the first four transmembrane segments (S1-S4) and assemble as a dimer with each subunit containing its own permeation pathway. The N-terminus and C-terminus of Hv1 are on the cytoplasmic side. The main region of attachment of the Hv1 channel dimer is in the intracellular C-terminus.

Hv1 from several multicellular species (human, mouse, and the sea squirt Ciona intestinalis) exist as dimers, whereas Hv1 in several unicellular species are predicted to exist as monomers. When Hv1 from species with dimeric channels are forced to express as monomers, the channels open (activate) several-fold faster than dimeric forms and their g_(H)-V relationship is somewhat (10-15 mV) more positive. The promoters of each monomer in an Hv1 channel dimer gate cooperatively, such that both promoters must undergo voltage-induced conformational change before either conduction pathway is open. Consequently, the probability that dimeric Hv1 will open is more dependent on voltage compared to the monomeric form.

Certain amino acids may be important for Hv1 selectivity for protons. The acidic amino acid aspartate at position 112 (Asp112), which is located in the middle of the S1 transmembrane helix, is one such amino acid important for Hv1 proton selectivity. Mutating Asp112 to any other amino acid except Glu (another acidic amino acid) converts hHv1 channel into an anion channel. Asp112 interacts with arginine (Arg208) in the S4 segment via two hydrogen bonds, with Asp or Arg protonated. Introducing a hydronium ion, H3O⁺, into either configuration results in protonation of Asp, breaking of the hydrogen bonds, and resulting in a neutral water molecule that mediates interactions in AspH⁰—H₂O⁰-Arg⁺. From this protonated selectivity filter configuration, reprotonation of the water molecule results in net H⁺ permeation. Therefore, the unique abilities of protons to travel with a water molecule and to transfer readily and reversibly with other groups is exploited by Hv1 in achieving proton selectivity. Proton selectivity can also be preserved when Asp is replaced with Glu, or when Arg is replaced with Lys.

Besides the selectivity filter, there is another hydrophobic region in hHv1 predicted by molecular dynamic simulations. This second region is a highly conserved Phe150. The proton may inject its own water wire through this hydrophobic region. Thus, protons are uniquely able to open the selectivity filter and to hydrate dry regions of the pore.

Hv1 Channel Mechanism

Hv1 channels are uniquely selective for protons, with detectably no other ion permeation. The requirement of such selectivity is crucial because the concentration of protons in mammalian cells or bodily fluids is orders of magnitude lower than that of other major cations like Na⁺ and K⁺. As already discussed above, Hv1 channel selectivity is dependent on specific amino acids, including Asp112 and Arg208.

The primary determinants of Hv1 channel activation are transmembrane voltage and transmembrane pH gradient (ΔpH, defined as pH_(o)-pH_(i)). Hv1 opens at relatively positive transmembrane voltages (i.e. depolarization), but voltage-dependence is strongly modulated by pH. When the cytosol becomes more acidic relative to the extracellular or intraluminal space, the entire conductance-voltage relationship of the channel shifts by 40 mV to more negative voltages for each unit increase in ΔpH. Conversely, when the extracellular or intraluminal side becomes more acidic than the cytosol, the conductance-voltage relationship shifts by 40 mV to more positive voltages for each unitary change in ΔpH. Parameters that are useful in determining Hv1 channel activation include: (1) the membrane voltage (measured on the cytosolic side, relative to the extracellular or luminal side); (2) the cytosolic pH (whereby acidification favors activation at any given voltage); and (3) the extracellular or intra-luminal pH (whereby acidification opposes activation at any given voltage). Three charged Arg residues in the S4 transmembrane segment of Hv1 confer voltage dependency, while the structural basis for pH sensing is not fully understood.

Besides voltage and ΔpH, other parameters can also influence Hv1 channel activation. For example, phosphorylation of the channel by PKC can produce an enhanced responsiveness mode, allowing for more channels to open more quickly. PKC phosphorylates Hv1 at Thr29 located in the intracellular N-terminus. A situational example of enhanced gating of Hv1 is phagocyte exposure to pathogenic stimuli, such as bacteria. A diversity of stimuli can induce enhanced gating, including chemotactic peptides such as fMLF in neutrophils, lipopolysaccharide (LPS) in dendritic cells, IgE in basophils, IL-5 in eosinophils, and arachidonic acid in neutrophils and eosinophils. Such enhanced Hv1 gating is only functional in certain cells. The intensity of enhanced gating response may be associated with the presence of an active NADPH oxidase complex. Additionally, slower tail current decay (channel closing), is temporally correlated with NADPH oxidase activity. Enhanced gating makes Hv1 channels more likely to open or remain open, thereby requiring a smaller stimulus to activate H⁺ flux. Hv1 proton currents are also sensitive to temperature, and have a small (15 fF) unitary conductance.

Hv1 Channel Expression

Hv1 channels have been identified directly by voltage-clamp recordings in many primary tissue cell types, including neutrophils, basophils, eosinophils, cardiac fibroblasts, cultured myotubes, tracheal epithelium, and monocytes. Neutrophil and eosinophil granulocytes express the highest levels of Hv1.

In most cells, Hv1 is expressed in plasma membranes, though there is evidence that Hv1 can also be expressed on intracellular membranes such as Golgi membranes in some cells. Full-length Hv1 can be detected in human granulocytes by western blot as a 30 kDa monomer or 70 kDa dimer. Based on immunocytochemistry, Hv1 partially colocalizes with NOX2 in the membrane of intracellular granules and in the plasma membrane.

Hv1 Channel Functions

Functions of Hv1 channels differ depending on the cells in which they are expressed. Cells in which high activity and a physiological function for Hv1 channels have been documented include immune cells, central nervous system cells, airway epithelia, spermatozoa, and cardiac fibroblasts. Under normal circumstances, when Hv1 channels open, H⁺ efflux occurs and thereby increases pH_(i), decreases pH_(o) and hyperpolarizes the membrane potential. These changes can have different consequences in different cells.

In some cells, Hv1 channel expression and function is closely linked to expression and function of the enzyme NADPH oxidase (NOX), of which there are four isoforms: NOX1, NOX2, NOX3 and NOX4. NOX is a membrane-bound enzyme that transfers electrons from NADPH across cell membranes and couples these electrons to molecular oxygen to produce superoxide anion. In some locations, superoxide can undergo further reactions to generate reactive oxygen species (ROS). One of the functions of Hv1 linked to NOX activity is the extrusion of protons to compensate for the loss of electrons, as discussed in more detail below.

Hv1 expression and/or function has been detected in both innate and adaptive immune cells. A major role of Hv1 channels is in the phagosome, an intracellular organelle in white blood cells where pathogens such as bacteria are engulfed and destroyed. The primary role for Hv1 channels in the phagosome is to allow NOX2 (the NADPH oxidase enzyme complex) to produce large quantities of reactive oxygen species (ROS) to kill pathogens, in a process called “respiratory burst”. During the respiratory burst, NOX enzymes catalyze the transfer of electrons from NADPH across the plasma membrane to reduce molecular oxygen to O²⁻, generating two protons in the cytoplasm. The resulting depolarization and cytoplasmic acidification inhibits NOX2 activity. Depolarization opens Hv1 channels to sustain NOX2 activity by extruding protons from the cytoplasm, thereby maintaining physiological membrane potential and re-establishing normal pH. Such contributions of Hv1 channels to NOX2-dependent ROS release are characterized in granulocytes and in particular neutrophils. H⁺ current has also been detected in basophils. In these cells, IgE stimulates Hv1 channels, which facilitate release of histamine. Hv1 may also participate in ROS production and/or histamine release by mast cells.

B lymphocytes of the adaptive immune system, which are responsible for antibody production, express Hv1 protein. It has been suggested that Hv1 mediates signaling in the antibody maturation process upon B-cell receptor activation by antigen binding. For example, Hv1 channels may be required for ROS production by NOX2 in mature B lymphocytes upon antigen stimulation. Given the involvement of Hv1 in B cell receptor signaling, inhibitors of Hv1 may be useful for treating autoimmune diseases and B cell malignancies.

Hv1 channels are also expressed in T lymphocytes, which are cells of the adaptive immune system that recognize antigens presented by major histocompatibility complex I or II. Here, Hv1 may function to facilitate ROS production and help regulate the number of activated T lymphocytes, thereby opposing an autoimmune phenotype.

Expression and activity of Hv1 has been confirmed in human sperm. Functional data indicate that Hv1 activity may be necessary for sperm activation and mobility of human sperm to achieve fertilization. The process that prepares sperm to fertilize an oocyte is called capacitation, a kind of maturation process that is triggered by an increase in intracellular pH and ROS. Changes related to capacitation include: changes in sperm motility, decrease of cholesterol in the membranes, increase of tyrosine phosphorylation in several proteins, and maturation of the sperm response to progesterone. Interestingly, seminal fluid has an unusually high concentration of Zn²⁺ (which is known to inhibit Hv1), whereas the female reproductive tract has low Zn²⁺ concentrations. It is hypothesized that on arrival of sperm in the female reproductive tract, Hv1 becomes activated and cooperates with the sperm-specific Ca²⁺ channel CatSper and NOX5 to activate sperm effector functions such as sperm movement, capacitation, sperm-zona pellucida interaction, acrosome reaction, and sperm-oocyte fusion.

There is evidence to suggest the presence of Hv1 channels in mammalian brain tissue. Without wishing to be bound by any particular theory, the present disclosure proposes that Hv1 channels may play a neuroprotective role by extruding protons from metabolically active neurons and regulating neuronal pH homeostasis. Hv1 expression has been detected in human microglia, the macrophage-like cells of the central nervous system. Hv1 in microglia may contribute to CNS disease by supporting NOX function. Microglia can become activated in acute and chronic brain disorders including brain injury, ischemia, and neurodegeneration. The expression and function of Hv1 is correlated with the expression and function of NOX2. Hv1 channels may support the activity of NOX2 in microglia by extruding excess protons from the cytoplasm. Oxidative stress, at least in part due to ROS generation by NOX, can contribute to the development of CNS disease. Hv1 inhibition could be beneficial for the treatment of neurodegenerative processes accompanied by excessive production of ROS by microglia, such as stroke, Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis, among others.

The present disclosure proposes that NOX-independent Hv1 channel functions may also exist, given that certain cell types (e.g., basophil granulocytes) that exhibit Hv1 channel activity are not known to express NOX.

Evidence indicates that Hv1 also functions in airway epithelia (e.g. tracheal epithelia) in functions such as providing a protective mechanism through acidification of the airway surface liquid. Hv1 may also function in cardiac fibroblasts, though its function in these cells is not fully known. Some experimental data also suggests Hv1 function in monocytes and macrophages. Hv1 channels may promote osteoclast cell function, for instance by promoting bone resorption by osteoclast cells. Hv1 channels may also mediate antigen presentation by dendritic cells.

Many other tissues and cells not mentioned here also express Hv1 channels, some at relatively low levels. For most of the cell types and tissues that have been reported to express low levels of Hv1 channels, a specific function has not been assigned.

Given the widespread expression and function of Hv1 channels, it may not be surprising that channel dysfunction can cause or enhance pathologic states. Moreover, genomic studies have identified the HVCN1 gene as being relevant to multiple diseases. For example, HVCN1 has been associated with Crohn's disease activity and cystic fibrosis. A study in HVCN1 knockout rats indicated that Hv1 may contribute to the development of hypertension and renal disease with a high-salt diet. The link between Hv1 function and ROS production provides some insight on the mechanism of some Hv1-associated disorders. Excessive ROS production is thought to cause local tissue damage and contribute to several pathological conditions, including atherosclerosis, ischemic stroke, Parkinson's disease, ischemic liver disease, Alzheimer's disease, and aging. A study on ischemic stroke has confirmed that Hv1 can exacerbate brain damage by facilitating production of ROS by NOX in microglia. Moreover, it was recently shown that Hv1-deficient mice are protected in models of stroke, suggesting that pharmacological inhibition of Hv1 channels may have neuroprotective benefits (see Seredenina, T., et al. “Voltage-gated proton channels as novel drug targets: from NADPH oxidase regulation to sperm biology.” Antioxid Redox Signal. 10; 23(5): 490-513 (2015) and references cited therein).

Hv1 channels may contribute to the malignancy of several cancers, including breast cancer, colorectal cancer and leukemia. For example, higher levels of Hv1 expression occur in breast cancer cell lines with greater metastatic likelihood and knockdown of Hv1 in breast cancer cell lines reduced proliferation and invasiveness. In human patients, a high level of Hv1 expression was correlated with poor prognosis. One mechanism by which Hv1 contributes to cancer cell malignancy is related to the abnormal metabolism of cancer cells, which use glycolysis in preference to oxidative phosphorylation even in the presence of adequate oxygen. This altered metabolism creates a buildup of lactic acid that acidifies the cells, thus requiring enhanced activity of H⁺ extrusion to prevent cell death.

The particular isoform of Hv1 that is expressed may contribute to certain malignancies. The levels of the short isoform of Hv1 are higher in malignant B cell lines as compared to normal B lymphocytes. Moreover, the short isoform comprises approximately one-third of the Hv1 protein in malignant B cells from patients with chronic lymphocytic leukemia. The enhanced gating response is substantially more pronounced in the short compared to the long isoform of Hv1. Hv1 channel activity, proliferation and cell migration are all promoted by the expression of the short isoform.

Hv1 Channel Modulators

Modulation of Hv1 channel activity is an attractive strategy for treating Hv1-related pathologies, including the ones described above. For example, agents that modulate Hv1 may be expected to ameliorate inflammation, allergies, autoimmunity, cancer, asthma, brain damage from ischemic stroke, Alzheimer's disease, infertility, and numerous other conditions. Depending on the disease and affected tissue, either Hv1 activation or inhibition could prove useful. However, clinically compatible Hv1 modulators are not known. Therefore, there is an unmet need in identifying potent and selective modulators of Hv1.

One of the challenges in creating modulators of Hv1 channels stems from the channel structure. The extracellular loops of hHv1 are fewer than a dozen amino acids, resulting in a relatively small extracellular portion of the Hv1 molecule to which drugs can bind. For example, this limits the epitope possibilities for antibodies to bind externally. Additionally, inhibition of Hv1 by physical occlusion is also a challenge, since the channel is structured to be closely packed and prevent other ions from permeating.

In some instances, such as autoimmune disease and male infertility, Hv1 activation may be an attractive pharmacological strategy. Unsaturated long-chain fatty acids such as oleic acid and arachidonic acid have been shown to enhance Hv1 proton currents. This appears to be a direct pharmacological activation of Hv1. Arachidonic acid has been observed to activate a proton conductance in phagocytes. However, arachidonic acid can also activate multiple signaling pathways, which in certain cases can lead to activation of NOX enzymes and therefore indirectly activate H⁺ currents. Activators of enhanced gating can also enhance Hv1 function. In general, ion channel activators are more difficult to identify than inhibitors since binding to the channel usually produces inhibition.

Zn²⁺ and other polyvalent cations are known to inhibit Hv1 channels. Hv1 channels can be blocked by Zn²⁺ at concentrations ranging from 100 nM to 1 mM depending on the extracellular pH and on the presence of other polyvalent cations. The mechanism by which Zn²⁺ inhibits Hv1 involves Zn²⁺ competing with H⁺ for binding to the external surface of Hv1 channels. Two His residues (His140 and His193) located at the interface between the channel monomers coordinate Zn²⁺ in the closed channel and thereby oppose channel opening. This mechanism changes the membrane potential perceived by the channel, and therefore requires stronger voltage to elicit proton current. Zn²⁺ shifts the current-voltage relationship positively and slows the kinetics of Hv1 channel activation. However, Zn²⁺ ions are implicated in many other physiological processes, and therefore the usefulness of Zn²⁺ as a specific H⁺ channel blocker is limited.

There are no documented high-affinity blockers of Hv1 channels that originate in venom or toxin. Tarantula toxins, including hanatoxin, can inhibit Hv1 at low micromolar concentrations by interacting with the S3 and S4 helices from the membrane interior and shifting the g_(H)-V relationship in the positive direction. However, hanatoxin is not specific for Hv1. Different voltage-sensing proteins, including Hv1 and other ion channels, contain the highly conserved voltage sensor regions composed of S3 and S4 helices, termed the paddle motif. Binding of hanatoxin to the paddle motif inhibits ion fluxes through various voltage-dependent ion channels besides Hv1.

Guanidine derivatives have been shown to inhibit depolarization-induced H⁺ current (see Seredenina, T., et al. “Voltage-gated proton channels as novel drug targets: from NADPH oxidase regulation to sperm biology.” Antioxid Redox Signal. 10; 23(5): 490-513 (2015); DeCoursey, T. E. “The voltage-gated proton channel: a riddle, wrapped in a mystery, inside an enigma.” Biochemistry 54(21): 3250-68 (2015); and references cited therein). The derivative 2GBI [2-guanidinobenzimidazole (IC₅₀=38 μM)] was found to have an intracellular site of action and to only bind when the channel was open. Other identified derivatives include 1-(1,3-benzothiasol-2-yl)guanidine and 5-chloro-2-guanidinobenzimidazole. Guanidine derivatives have shown neuroprotective potential in an in vitro model of ischemia. The biggest challenge for pharmaceutical application of guanidine derivatives is their intracellular site of action.

Several other compounds have been observed to block H⁺ currents. Examples of such other compounds include weak bases (e.g. 4-aminopyridine, amiloride, verapamil or D600), tricyclic antidepressants (imipramine, amitryptiline, and desipramine), the selective serotonin reuptake inhibitor fluoxetine, the morphine-derivative dextromethorphan (DM), and a tea catechin flavonoid EGCG. These other potential inhibitors have several drawbacks, including mechanisms of action that do not directly involve Hv1 channels, multiple other targets, and effective concentrations that are too high to be of pharmaceutical interest.

To-date, there are no selective inhibitors of Hv1 channels. There is an unmet need to develop such inhibitors, especially ones that are compatible with clinical use.

Hv1 Modulating Agents Hv1 Modulating Agent Activities

The present disclosure provides agents that modulate Hv1. Among other things, the present disclosure provides agents that, for example, modulate one or more Hv1 activities when contacted with an Hv1 channel, for example, in vitro and/or in vivo. In some embodiments, Hv1 modulating agents modulate Hv1 activities of Hv1 monomers and dimers with similar IC₅₀. In some embodiments, Hv1 modulating agents specifically bind Hv1. In some embodiments, Hv1 modulating agents inhibit Hv1. In some embodiments, Hv1 modulating agents activate Hv1.

In some embodiments, Hv1 modulating agents do not physically occlude Hv1 channels. In some embodiments, Hv1 modulating agents bind to Hv1 but do not bind to other voltage-gated channels or other ion channels.

In some embodiments, Hv1 modulating agents bind to the external surface of Hv1. In some embodiments, Hv1 modulating agents target or bind to the S3-S4 external loop region of hHv1. For example, Hv1 modulating agents may bind to hHv1 at amino acid residues 1183 to L204. In some embodiments, Hv1 modulating agents bind to regions of hHv1 comprising an amino acid sequence corresponding to ILDIVLLFQEHQFEALGLLILL (SEQ ID NO: 111).

In some embodiments, Hv1 modulating agent binding to Hv1 is reversible. In some embodiments, Hv1 modulating agent binding to Hv1 may be irreversible. In some embodiments, Hv1 modulating agent binding to Hv1 is strong but not irreversible.

In some embodiments Hv1 modulating agents bind to open Hv1 channels. In some embodiments, Hv1 modulating agents bind to closed channels. In some embodiments, affinity of Hv1 modulating agents for closed states of Hv1 is about 1 nM. In some embodiments, affinity of Hv1 modulating agents is lower for open states of the channel (e.g. about 200 nM) as compared to closed states of the channel. In some embodiments, Hv1 modulating agents slow opening of closed states of Hv1 even as they unbind.

In some embodiments, provided Hv1 modulating agents may change transmembrane voltage of a cell. Hv1 modulating agents may hyperpolarize the membrane potential. Hv1 modulating agents may depolarize the membrane potential. Effects of Hv1 modulating agents may be measured by, for example, direct electrophysiological recordings of voltage-gated proton currents, such as patch-clamp recordings.

In some embodiments, provided Hv1 modulating agents are characterized in that, for example, they decrease or block proton current. In some embodiments, Hv1 modulating agents may reduce the number or likelihood of Hv1 channel opening. In some embodiments, Hv1 modulating agents may speed up the rate of Hv1 channel closing. In some embodiments, Hv1 modulating agents may cause an Hv1 channel to require stronger voltage to elicit proton current.

In some embodiments, provided Hv1 modulating agents are characterized in that, for example, they increase proton currents and/or slow the closing of Hv1 channels. In some embodiments, Hv1 modulating agents may provide an enhanced responsiveness mode, allowing more channels to open more quickly, increasing likelihood that Hv1 channels will open or remain open, and/or reducing the stimulus required to activate H⁺ flux.

In some embodiments, Hv1 modulating agents may increase or decrease proton (H⁺) current but do not directly alter current of other ions (e.g. Na⁺, K²⁺, Ca²⁺).

In some embodiments, Hv1 modulating agents may change the transmembrane pH gradient (ΔpH, defined as pH_(o)-pH_(i)). In some embodiments, provided Hv1 modulating agents may increase or decrease intracellular or cytosolic pH (pH_(i)). Thus, Hv1 modulating agents may decrease or increase the cytoplasmic acidity. In some embodiments, provided Hv1 modulating agents may increase or decrease the extracellular, intraluminal, or organelle pH (pH_(o)). Thus, Hv1 modulating agents may decrease or increase the extracellular, intraluminal, or organelle acidity.

In some embodiments, Hv1 modulating agents may increase or decrease cellular ROS production.

In some embodiments, Hv1 modulating agents may increase or decrease the function and/or activity of NOX enzymes, including NOX1, NOX2, NOX3, and/or NOX4. In some such embodiments, Hv1 modulating agents may enhance or reduce the ability of NOX enzymes to transfer electrons. In some such embodiments, Hv1 modulating agents may increase or decrease the production of superoxide anion by a cell. In some such embodiments, Hv1 modulating agents may increase or decrease the quantity of ROS production mediated by NOX enzymes. In some embodiments, Hv1 modulating agents may sustain NOX activity by extruding protons from the cytoplasm.

In some embodiments, Hv1 modulating agents may alter signaling pathways that can be affected by Hv1 activity. In some embodiments, Hv1 modulating agents may affect cellular, physiological, or pathological processes that can be affected by Hv1 activity. In some such embodiments, Hv1 modulating agents may influence inflammation, allergies, autoimmunity, cancer, asthma, brain damage from ischemic stroke, Alzheimer's disease, and fertility.

In some embodiments, Hv1 modulating agents may alter sperm activity or fertilization. Hv1 modulating agents may affect sperm mobility, capacitation, sperm-zona pellucida interaction, acrosome reaction, and sperm-oocyte fusion. In a particular example, Hv1 modulating agents inhibit properties associated with sperm capacitation.

In another example, Hv1 modulating agents may alter the ability of white blood cells to fight infections. Hv1 modulating agents may alter the activity of phagosomes, NOX enzymes, or ROS production. In a particular example, Hv1 modulating agents may decrease ROS production in white blood cells.

Hv1 Modulating Agent Structure

In some embodiments, an Hv1 modulating agent is or comprises a polypeptide. In some embodiments, a polypeptide component of an Hv1 modulating agent is 10-100 amino acids in length.

In many embodiments in which a provided Hv1 modulating agent includes a polypeptide component, the polypeptide component of the agent has an amino acid tertiary structure that is characterized as an inhibitor cysteine knot (ICK)-like structural motif. In some embodiments, a polypeptide component has a structure that has substantial structural similarity to an ICK structural motif. In some embodiments, a polypeptide component has three disulfide bridges. In some embodiments, a polypeptide component has three beta strands. In some embodiments, a polypeptide component has an amino acid sequence with six conserved cysteine residues of an ICK motif (FIG. 1).

In many embodiments in which a provided Hv1 modulating agent includes a polypeptide component, the polypeptide component of the agent has an amino acid sequence that includes one or more elements that is substantially identical to, but different from, that of wild-type toxin sequences (e.g., of a wild-type voltage sensor toxin). In some embodiments, such a sequence element has a length of about 5 to about 20 amino acids. In some embodiments, such a sequence element shows at least 40%, 50%, 60%, 70%, 80%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100% sequence identity with a corresponding element of a wild-type toxin. In some embodiments, a polypeptide component of a provided Hv1 modulating agent may show significant (e.g., at least 40%, 50%, 60%, 70%, 80%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, or higher) overall sequence identity with, while differing from, a wild-type toxin. In some embodiments, a polypeptide component has an amino acid sequence that includes a plurality of toxin sequence elements, each of which is substantially identical to a sequence element that is found in the same, or a different, reference wild-type toxin. In some such embodiments, the plurality of toxin sequence elements are assembled in linear order so that the amino acid sequence shows overall correspondence with (e.g., shares one or more certain structural features, such as number and/or [relative] location of one or more cysteine residues) a full-length toxin. In some embodiments, a polypeptide component has an amino acid sequence that includes one or more residues found in a wild-type toxin that participates in binding by that wild-type toxin to a voltage-sensing protein.

Exemplary wild-type toxin sequences are presented in Table 1. In some embodiments, a wild-type toxin is a venom toxin. In some embodiments, a venom toxin is a toxin found in venom of organisms such as scorpion (e.g., Pandinus imperator), sea anemone, snails (e.g. Conus marmoreus), snakes, and spiders (e.g., Grammostola rosea).

TABLE 1 SEQ NCBI ID Toxin Accession NO: Name Sequence NO: Animal Species 1 HwTx-IV ECLEIFKACNPSNDQCCKSSKLVCSRKTRWCKYQI P83303.2 Haplopelma schmidti (Chinese bird spider) 2 HnTx-IV ECLGFGKGCNPSNDQCCKSSNLVCSRKHRWCKYEI D2Y232.1 Haplopelma hainanum (Chinese bird spider) 3 HnTx-V ECLGFGKGCNPSNDQCCKSANLVCSRKHRWCKYEI P60975.1 Haplopelma hainanum (Chinese bird spider) 4 PaurTx3 DCLGFLWKCNPSNDKCCRPNLVCSRKDKWCKYQI P84510.1 Paraphysa scrofa (Chilean copper tarantula) 5 CcoTx1 DCLGWFKSCDPKNDKCCKNYTCSRRDRWCKYDL P84507.1 Ceratogyrus marshalli (Straighthorned baboon tarantula) 6 CcoTx2 DCLGWFKSCDPKNDKCCKNYTCSRRDRWCKYYL P84508.1 Ceratogyrus marshalli (Straighthorned baboon tarantula) 7 VSTX3 DCLGWFKGCDPDNDKCCEGYKCNRRDKWCKYKLW P0C2P5.1 Grammostola rosea (Chilean rose tarantula) 8 T1Tx1 AACLGMFESCDPNNDKCCPNRECNRKHKWCKYKLW P83745.1 Theraphosa blondi (Goliath birdeating spider) 9 JZTX-25 DDCLGMFSSCNPDNDKCCEGRKCDRRDQWCKWNPW B1P1F1.1 Chilobrachys guangxiensis (Chinese earth tiger tarantula) 10 JZTX-27 DCLGLFWICNYMDDKCCPGYKCERSSPWCKIDI B1P1H2.1 Chilobrachys guangxiensis (Chinese earth tiger tarantula) 11 T1Tx3 DDCLGMFSSCDPNNDKCCPNRVCRVRDQWCKYKLW P83747.1 Theraphosa blondi (Goliath birdeating spider) 12 T1Tx2 DDCLGMFSSCDPKNDKCCPNRVCRSRDQWCKYKLW P83746.1 Theraphosa blondi (Goliath birdeating spider) 13 HwTx-I ACKGVFDACTPGKNECCPNRVCSDKHKWCKWKL P56676.2 Haplopelma schmidti (Chinese bird spider) 14 GsMTx4 GCLEFWWKCNPNDDKCCRPKLKCSKLFKLCNFSFGK Q7YT39.1 Grammostola rosea (Chilean rose tarantula) 15 Omega- ADCGWLFHSCESNADCCENWACATTGRFRYLCKYQI P81595.1 Hadronyche versuta AcTx- (Blue mountains Hv1b funnel-web spider) 16 IpTxa GDCLPHLKRCKADNDCCGKKCKRRGTNAEKRCR P59868.1 Pandinus imperator (Emperor scorpion) 17 VSTX1 ECGKFMWKCKNSNDCCKDLVCSSRWKWCVLASPF P60980.2 Grammostola rosea (Chilean rose tarantula) 18 HnTx-I ECKGFGKSCVPGKNECCSGYACNSRDKWCKVLL D2Y1X6.1 Haplopelma hainanum (Chinese bird spider) 19 Maurocalcine GDCLPHLKLCKENKDCCSKKCKRRGTNIEKRCR P60254.1 Scorpio maurus palmatus (Chactoid scorpion) 20 HpTX3 ECGTLFSGCSTHADCCEGFICKLWCRYERTW P58427.1 Heteropoda venatoria (Brown huntsman spider) 21 HNTX- ECRYWLGTCSKTGDCCSHLSCSPKHGWCVWDWTFRK D2Y2C3.1 Haplopelma VII hainanum (Chinese bird spider) 22 JZTX GCQKFFWTCHPGQPPCCSGLACTWPTEICIDG P0CH50.1 Chilobrachys F4- guangxiensis 32.60 (Chinese earth tiger tarantula) 23 HnTx- GCKGFGDSCTPGKNECCPNYACSSKHKWCKVYL D2Y1X9.1 Haplopelma III hainanum (Chinese bird spider) 24 Toxin_KJ1 DDCGTLFSGCDTSKDCCEGYVCHLWCKYK P61791.1 Heteropoda venatoria (Brown huntsman spider) 25 ScTx1 DCTRMFGACRRDSDCCPHLGCKPTSKYCAWDGTI P60991.1 Stromatopelma calceatum (Featherleg baboon tarantula) 26 JZTX-50 RCIEEGKWCPKKAPCCGRLECKGPSPKQKKCTRP B1P1B0.1 Chilobrachys guangxiensis (Chinese earth tiger tarantula) 27 ProTx-1 ECRYWLGGCSAGQTCCKHLVCSRRHGWCVWDGTFS P83480.1 Thrixopelma pruriens (Peruvian green velvet tarantula) 28 HmTx1 ECRYLFGGCSSTSDCCKHLSCRSDWKYCAWDGTFS P60992.1 Heteroscodra maculata (Togo starburst tarantula) 29 GxTx1E EGECGGFWWKCGSGKPACCPKYVCSPKWGLCNFPMP P84835.1 Chilobrachys guangxiensis (Chinese earth tiger tarantula) 30 GxTX-1D DGECGGFWWKCGSGKPACCPKYVCSPKWGLCNFPMP P84836.1 Chilobrachys guangxiensis (Chinese earth tiger tarantula) 31 Omega- DDDCGWIMDDCTSDSDCCPNWVCSKTGFVKNICKYEM P56207.1 Hadronyche versuta AcTx- (Blue mountains Hv1a funnel-web spider) 32 JZTX LCSREGEFCYKLRKCCAGFYCKAFVLHCYRN P0CH55.1 Chilobrachys F7- guangxiensis 15.33 (Chinese earth tiger tarantula) 33 Tx2-9 SFCIPFKPCKSDENCCKKFKCKTTGIVKLCRW AAB32862.1 Brachypelma smithii (Mexican red knee tarantula) 34 GxTX-2 ECRKMFGGCSVDSDCCAHLGCKPTLKYCAWDGT P84837.1 Chilobrachys guangxiensis (Chinese earth tiger tarantula) 35 HpTX1 DCGTIWHYCGTDQSECCEGWKCSRQLCKYVIDW P58425.1 Heteropoda venatoria (Brown huntsman spider) 36 SHLP-I GCLGDKCDYNNGCCSGYVCSRTWKWCVLAGPWRR Q86C51.1 Haplopelma schmidti (Chinese bird spider) 37 JZTX- GCGGLMAGCDGKSTFCCSGYNCSPTWKWCVYARP P0C2X7.2 Chilobrachys VII guangxiensis (Chinese earth tiger tarantula) 38 JZTX-29 ECRKMFGGCSVHSDCCAHLGCKPTLKYCAWDGTF B1P1E4.1 Chilobrachys guangxiensis (Chinese earth tiger tarantula) 39 JZTX- GCGGLMDGCDGKSTFCCSGFNCSPTWKWCVYARP B1P1C4.1 Chilobrachys 12.1 guangxiensis (Chinese earth tiger tarantula) 40 Toxin_AU2 DDCGGLFSGCDSNADCCEGYVCRLWCKYKL P61792.1 Heteropoda venatoria (Brown huntsman spider) 41 HaTx1 ECRYLFGGCKTTSDCCKHLGCKFRDKYCAWDFTFS P56852.1 Grammostola rosea (Chilean rose tarantula) 42 HaTx2 ECRYLFGGCKTTADCCKHLGCKFRDKYCAWDFTFS P56853.1 Grammostola rosea (Chilean rose tarantula) 43 VaTx1 SECRWFMGGCDSTLDCCKHLSCKMGLYYCAWDGTF P0C244.1 Psalmopoeus cambridgei (Trinidad chevron tarantula) 44 JzTx-XI ECRKMFGGCSVDSDCCAHLGCKPTLKYCAWDGTFGK P0C247.2 Chilobrachys guangxiensis (Chinese earth tiger tarantula) 45 HmTx2 ECRYFWGECNDEMVCCEHLVCKEKWPITYKICVWDRT P60993.1 Heteroscodra F maculata (Togo starburst tarantula) 46 JzTx- DGECGGFWWKCGRGKPPCCKGYACSKTWGWCAVEAP P62520.1 Chilobrachys III guangxiensis (Chinese earth tiger tarantula) (Chilobrachys jingzhao) 47 PcTx1 EDCIPKWKGCVNRHGDCCEGLECWKRRRSFEVCVPKT P60514.1 Psalmopoeus PKT cambridgei (Trinidad chevron tarantula) 48 Agelenin GGCLPHNRFCNALSGPRCCSGLKCKELSIWDSRCL P31328.1 Allagelena opulenta (Funnel weaving spider) 49 JZTX-13 QCGEFMWKCGAGKPTCCSGYDCSPTWKWCVLKSPGRR B1P1C9.1 Chilobrachys guangxiensis (Chinese earth tiger tarantula) 50 JZTX-15 TCYDIGELCSSDKPCCSGYYCSPRWGWCIYSTRGGR B1P1D4.1 Chilobrachys guangxiensis (Chinese earth tiger tarantula) 51 Omega- SAVCIPSGQPCPYSKYCCSGSCTYKTNENGNSVQRCD P81599.1 Hadronyche versuta AcTx- (Blue mountains Hv1f funnel-web spider) 52 HNTX- CAAEGIPCDPNPVKDLPCCSGLACLKPTLHGIWYKHH D2Y299.1 Haplopelma XIX YCYTQ hainanum (Chinese bird spider) 53 lamda- GCNRKNKKCNSDADCCRYGERCISTKVNYYCRPDRGP P86399.2 Mesobuthus eupeus MeuTx (Lesser Asian scorpion) 54 JZTX-24 VCRGYGLPCTPEKNDCCQRLYCSQHRLCSVKA B1P1F0.1 Chilobrachys guangxiensis (Chinese earth tiger tarantula) 55 HwTx-X KCLPPGKPCYGATQKIPCCGVCSHNKCT P68424.2 Haplopelma schmidti (Chinese bird spider) 56 JZTX-21 CGGWMAKCADSDDCCETFHCTRFNVCGK B1P1E6.1 Chilobrachys guangxiensis (Chinese earth tiger tarantula) 57 magi-11 SCKLTFWRCKKDKECCGWNICTGLCIPP Q75WH2.1 Macrothele gigas (Spider) 58 SGTx1 TCRYLFGGCKTTADCCKHLACRSDGKYCAWDGTF P56855.1 Stromatopelma calceatum griseipes (Feather leg baboon tarantula) 59 JZTX-44 ECKWYLGDCKAHEDCCEHLRCHSRWDWCIWDGTF B1P1G8.1 Chilobrachys guangxiensis (Chinese earth tiger tarantula) 60 HNTX-VI ECKYLWGTCEKDEHCCEHLGCNKKHGWCGWDGTF P0CH70 Haplopelma hainanum (Chinese bird spider) 61 GsAF_I YCQKWLWTCDSERKCCEDMVCRLWCKKRL P61408.1 Grammostola rosea (Chilean rose tarantula) 62 GrTx1 YCQKWMWTCDSKRKCCEDMVCQLWCKKRL P85117.1 Grammostola rosea (Chilean rose tarantula) 63 PaTX1 YCQKWMWTCDSARKCCEGLVCRLWCKKII P61230.1 Paraphysa scrofa (Chilean copper tarantula) 64 Magi-5 GCKLTFWKCKNKKECCGWNACALGICMPR P83561.2 Macrothele gigas (Spider) 65 HwTx-V ECRWYLGGCSQDGDCCKHLQCHSNYEWCVWDGTFSK P0C245.1 ECRWYLGGCSQDGDCCKH LQCHSNYEWCVWDGTFSK 66 VaTx2 GACRWFLGGCKSTSDCCEHLSCKMGLDYCAWDGTF P0C245.1 Psalmopoeus cambridgei (Trinidad chevron tarantula) 67 SNX482 GVDKAGCRYMFGGCSVNDDCCPRLGCHSLFSYCAWDL P56854.1 Hysterocrates TFSD gigas (African tarantula) 68 PnVIIA DCTSWFGRCTVNSECCSNSCDQTYCELYAFPSFGA P56711.2 Conus pennaceus (Feathered cone) 69 PNTx27C4 IACAPRFSLCNSDKECCKGLRCQSRIANMWPTFCSQ P83996.2 Phoneutria nigriventer (Brazilian armed spider) 70 PRTx27C3 IACAPRGLLCFRDKECCKGLTCKGRFVNTWPTFCLV P83892.1 Phoneutria reidyi (Brazilian Amazonian armed spider) 71 JZTX-36 DCRKMFGGCSKHEDCCAHLACKRTFNYCAWDGSFSK B1P1D7.1 Chilobrachys guangxiensis (Chinese earth tiger tarantula) 72 JZTX-38 ECRWLFGGCEKDSDCCEHLGCRRAKPSWCGWDFTV B1P1G2.1 Chilobrachys guangxiensis (Chinese earth tiger tarantula) 73 JZTX-39 ECRWLFGGCEKDSDCCEHLGCRRAKPSWCGWDFTF B1P1G4.1 Chilobrachys guangxiensis (Chinese earth tiger tarantula) 74 PRTx26An0C3 IACAPRFSICNSDKECCKGLRCQSRIANMWPTFCLV P86418.1 Phoneutria nigriventer (Brazilian armed spider) 75 HNTX- CIGEGVPCDENDPRCCSGLVCLKPTLHGIWYKSYYCY D2Y253.1 Haplopelma XVI KK hainanum (Chinese bird spider) 76 HNTX- DCAGYMRECKEKLCCSGYVCSSRWKWCVLPAPWRR D2Y240.1 Haplopelma VIII hainanum (Chinese bird spider) 77 HNTX-IX ECRWYLGGCSQDGDCCKHLQCHSNYEWCIWDGTFSK D2Y236.1 Haplopelma hainanum (Chinese bird spider) 78 F5- ECKKLFGGCTTSSECCAHLGCKQKWPFYCAWDWSF P0CH51.1 Chilobrachys 21.66 guangxiensis (Chinese earth tiger tarantula) 79 Hm-2 GCIPSFGECAWFSGESCCTGICKWVFFTSKFMCRRVW P85506.1 Heriaeus melloteei GKD (Crab spider) 80 HdCa SEKDCIKHLQRCRENKDCCSKKCSRRGTNPEKRCR B8QG00.1 Hadrurus gertschi (Scorpion) 81 ProTx-2 YCQKWMWTCDSERKCCEGMVCRLWCKKKLW P83476.1 Thrixopelma pruriens (Peruvian green velvet tarantula) 82 JzTx-V YCQKWMWTCDSKRACCEGLRCKLWCRKIIG Q2PAY4.1 Chilobrachys guangxiensis (Chinese earth tiger tarantula) 83 HpTX2 DDCGKLFSGCDTNADCCEGYVCRLWCKLDW P58426.1 Heteropoda venatoria (Brown huntsman spider) 84 GsAF_II YCQKWMWTCDEERKCCEGLVCRLWCKKKIEW P61409.2 Grammostola rosea (Chilean rose tarantula) (Grammostola spatulata) 85 MrvIB ACSKKWEYCIVPILGFVYCCPGLICGPFVCV AAB34194.1 Conus marmoreus (Marble cone) 86 GsMTx-2 YCQKWMWTCDEERKCCEGLVCRLWCKRIINM P60273.1 Grammostola rosea (Chilean rose tarantula) 87 VSTX2 YCQKWMWTCDEERKCCEGLVCRLWCKKKIEEG P0C2P4.1 Grammostola rosea (Chilean rose tarantula) 88 JZTX-2 GCGTMWSPCSTEKPCCDNFSCQPAIKWCIWSP B1P189.1 Chilobrachys guangxiensis (Chinese earth tiger tarantula) 89 VaTx3 ECRWYLGGCKEDSECCEHLQCHSYWEWCLWDGSF P0C246.1 Psalmopoeus cambridgei (Trinidad chevron tarantula) 90 CcoTx3 GVDKEGCRKLLGGCTIDDDCCPHLGCNKKYWHCGWDG P84509.1 Ceratogyrus TF marshalli (Straighthorned baboon tarantula) 91 JZTX-IV ECTKFLGGCSEDSECCPHLGCKDVLYYCAWDGTFGK P0CH56.1 Chilobrachys guangxiensis (Chinese earth tiger tarantula) 92 JzTx-IX ECTKLLGGCTKDSECCPHLGCRKKWPYHCGWDGTF B1P1F5.2 Chilobrachys guangxiensis (Chinese earth tiger tarantula) 93 AcTx- SPTCIPSGQPCPYNENCCSQSCTFKENENGNTVKRCD P56207.1 Hadronyche versuta Hv1 (Blue mountains funnel-web spider) (Atrax versutus) 94 JZTX-34 ACREWLGGCSKDADCCAHLECRKKWPYHCVWDWTV B1P1F7.1 Chilobrachys guangxiensis (Chinese earth tiger tarantula) 95 Omega- SVCIPSGQPCPYNEHCCSGSCTYKENENGNTVQRCD P83580.2 Atrax robustus AcTx- Ar1a 96 Omega- SSTCIPSGQPCPYNENCCSQSCTYKENENGNTVKRCD P81595 Hadronyche versuta hexatoxin- (Blue mountains Hv1b funnel-web spider) 97 Omega- STCTPTDQPCPYHESCCSGSCTYKANENGNQVKRCD P0C2L4.1 Hadronyche AcTx- formidabilis Hi1a (Northern tree funnel-web spider) 98 Omega- SPTCIRSGQPCPYNENCCSQSCTFKTNENGNTVKRCD P0C2L4.1 Hadronyche AcTx- formidabilis Hf1a (Northern tree funnel-web spider) 99 Omega- SPTCIPTGQPCPYNENCCSQSCTYKANENGNQVKRCD P0C2L6.1 Hadronyche infensa AcTx- (Fraser island Hi1b funnel-web spider) 100 Omega- SSTCIRTDQPCPYNESCCSGSCTYKANENGNQVKRCD P0C2L7.1 Hadronyche infensa AcTx- (Fraser island Hi1c funnel-web spider) 101 Omega- SSTCIPSGQPCPYNENCCSQSCTFKENENGNTVKRCD P81596.1 Hadronyche versuta AcTx- (Blue mountains Hv1c funnel-web spider) 102 Omega- SPTCIPSGQPCPYNENCCSKSCTYKENENGNTVQRCD P81597.1 Hadronyche versuta AcTx- (Blue mountains Hv1d funnel-web spider) 103 Omega- SPTCIPSGQPCPYNENCCSQSCTYKENENGNTVKRCD P81598.1 Hadronyche versuta AcTx- (Blue mountains Hv1e funnel-web spider) 104 magi-1 CMGYDIHCTDRLPCCFGLECVKTSGYWWYKKTYCRRK P83557.1 Macrothele gigas S (Spider) 105 Omega- SPVCTPSGQPCQPNTQPCCNNAEEEQTINCNGNTVYR P83588.1 Missulena bradleyi MSTX- CA (Eastern mouse Mb1a spider) 106 F3- SPVCTP5GQPCQPNTQPCCNNAEEEQTINCNGNTVYR P0CH70.1 Haplopelma 24.71 CA hainanum (Chinese bird spider) 107 JzTx- YCQKWMWTCDSERKCCEGYVCELWCKYNL P0C5X7.2 Chilobrachys XII guangxiensis (Chinese earth tiger tarantula) 108 JZTX- ACGQFWWKCGEGKPPCCANFACKIGLYLCIWSP B1P1B7.1 Chilobrachys 1.2 guangxiensis (Chinese earth tiger tarantula) 109 GrTx- DCVRFWGKC5QT5DCCPHLACK5KWPRNICVWDG5V P60590.2 Grammostola rosea SIA (Chilean rose tarantula) 110 JZTX-35 DCRALYGGCTKDEDCCKHLACRRTLPTYCAWDLTFP B1P1F9.1 Chilobrachys guangxiensis (Chinese earth tiger tarantula)

In some embodiments, a wild-type toxin sequence can be a predicted wild-type toxin sequence. In some embodiments, a predicted wild-type toxin sequence is identified in public protein databases. In some embodiments, a sequence element found in a wild-type toxin sequence is identified by isolating an amino acid sequence delineated by six conserved cysteine residues that form disulfide bridges in an ICK motif of a wild-type toxin sequence. In some embodiments, a known amino acid sequence of a wild-type toxin sequence can be used as a template to align amino acid sequences from public protein databases and identify predicted wild type-toxin sequences. In one example, the amino acid sequence of the Peruvian green velvet tarantula (Thrixopelma pruriens) is used as a template to identify predicted wild-type toxin sequences using basic local alignment search tools in public protein databases.

In some embodiments, a polypeptide component has an amino acid sequence that is substantially identical to a sequence set forth in Table 2. In some embodiments, a polypeptide component has an amino acid sequence that is substantially identical to a sequence set forth in Table 2 and an activating or inhibiting effect on Hv1 as set forth in Table 2B. In some embodiments, a polypeptide component has an amino acid sequence that is encoded by a nucleotide sequence that is substantially identical to a sequence set forth in Table 2C.

TABLE 2A SEQ ID NO: Name Sequence 115 A1 DCAGYMRECKKDKECCGWNICNRKH KWCKYKLW 116 A2 GCQMTFWKCNALDHNCCHGYAACGC KKIIVSARIA 117 A4 GGCLPHNRFCNPSNDQCCKSANLVC RLWCKKKIEGDP 118 A6, G2 GCKGFGDSCADSDDCCETFHCKWVF FTSKFMCRRVWGKD 119 B1 GCLGDKCADSDDCCETFHCKWVFFT SKFMCRRVWGKD 120 B2 SPTCIPSGQPCADSDDCCETFHCKW VFFTSKFMCRRVWGKD 121 B3 DEDCQPPGNFCXNTSDCCEHLXCPT TPRFPYLCQYXMG 122 B4 GACRWFLGGCTPEKNDCCQRLYCGP FVCV 123 B5 SPVCTPSGQPCRENKDCCSKKCKTT GIVKLCRW 124 B6 ACSKKWEYCTKDSECCPHLGCWKRR RSFEVCVPKTPKT 125 C1 RCIEEGKWCTKDEDCCKHLACNRKH KWCKYKLW 126 C2, F2 SPTCIRSGQPCADSDDCCETFHCKW VFFTSKFMCRRVWGKD 127 C3 STCTPTDQPCADSDDCCETFHCKWV FFTSKFMCRRWGKD 128 C5 GCKWYLGDCADSDDCCETFHCKWVF FTSKFMCRRVWGKD 129 C6, D5 SSTCIPSGQPCADSDDCCETFHCKW VFFTSKFMCRRVWGKD 130 D3 ACSKKWEYCKEKLCCSGYVCKRRGT NIEKRCRG 131 D4 ACGQFWWKCTSDSDCCPNWVCRLWC KYKL 132 D6, E2 CRYWLGGCSQDGDCCKHLQCSPRWG WCIYSTRGGR 133 E1 DCGTIWHYCTPEKNDCCQRLYCSPR KRLVHL 134 E3 IACAPRFSICDPKNDKCCPMRVCSD KHKWCKWKL 135 E4 SSTCIPSGQPCRENKDCCSKKCSDK HKWCKWKLG 136 E5 DGECGGFWWKCKNSNDCCKDLVCKE KWPITYKICVWDRTF 137 E6 IACAPRFSLCDTSKDCCEGYVCNRK HKWCKYKLW 138 F4 ECKGFGKSCADSDDCCETFHCKWVF FTSKFMCRRWGKD 139 F5 SPVCTPSGQPCADSDDCCETFHCKW VFFTSKFMCRRVWGKD 140 F6 DDCGGLFSGCTPGKNECCPNRVCKI GLYLCIWS 141 G1 GCLGDKCADSDDCCETFHCKWVFFT SKFMCRRWGKD 142 G3 CRYLFGGCAWFSGESCCTGICSPRW GWCIYSTRGGR 143 G4 GDCLPHLKLCNPNDDKCCRPKLKCS RRGTNPEKRCR 144 G6 DDCGTLFSGCPYSKYCCSGSCKRRG TNIEKRCR 145 H4 AAEGCLCDRCXHSGDCCEDFHCTCE FFMM

TABLE 2B SEQ Activator/ ID NO: Name Sequence Inhibitor 118 A6 GCKGFGDSCADSDDCCET ACTIVATOR FHCKWVFFTSKFMCRRVW GKD 119 B1 GCLGDKCADSDDCCETFH ACTIVATOR CKWVFFTSKFMCRRVWGK D 128 C5 GCKWYLGDCADSDDCCET ACTIVATOR FHCKWVFFTSKFMCRRVW GKD 129 C6 SSTCIPS6QPCADSDDCC INHIBITOR ETFHCKWVFFTSKFMCRR VWGKD 129 D5 SSTCIPSGQPCADSDDCC INHIBITOR ETFHCKWVFFTSKFMCRR VWGKD 126 F2 SPTCIRSGQPCADSDDCC ACTIVATOR ETFHCKWVFFTSKFMCRR VWGKD 118 G2 GCKGFGDSCADSDDCCET ACTIVATOR FHCKWVFFISKFMCRRVW GKD

TABLE 2C SEQ ID NO: Name Nucleotide Sequences 146 A1 GATTGCGCGGGCTATATGCGCGAAT GTAAAAAAGATAAAGAATGCTGCGG CTGGAACATTTGCAACCGCAAACAT AAATGGTGCAAATATAAACTGTGG 147 A2 GGCTGCCAAATGACCTTTTGGAAAT GTAACGCGCTGGATCACAACTGCTG CCATGGCTATGCCGCCTGTGGATGC AAAAAAATTATTGTATCCGCGAGAA TCGCG 148 A4 GGCGGCTGCCTGCCGCATAACCGCT TTTGTAACCCGAGCAACGATCAGTG CTGCAAAAGCGCGAACCTGGTGTGC CGCCTGTGGTGCAAAAAAAAAATTG AAGGGGATCCG 149 A6, GGCTGCAAAGGCTTTGGCGATAGCT G2 GTGCGGATAGCGATGATTGCTGCGA AACCTTTCATTGCAAATGGGTGTTT TTTACCAGCAAATTTATGTGCCGCC GCGTGTGGGGCAAAGAT 150 B1 GGCTGCCTGGGCGATAAATGTGCGG ATAGCGATGATTGCTGCGAAACCTT TCATTGCAAATGGGTGTTTTTTACC AGCAAATTTATGTGCCGCCGCGTGT GGGGCAAAGAT 151 B2 AGCCCGACCTGCATTCCGAGCGGCC AGCCGTGTGCGGATAGCGATGATTG CTGCGAAACCTTTCATTGCAAATGG GTGTTTTTTACCAGCAAATTTATGT GCCGCCGCGTGTGGGGCAAAGATGG AT 152 B3 GACGAAGATTGCCAACCGCCGGGCA ACTTTTGTANCAACACCAGCGATTG CTGCGAACATCTGNNCTGCCCGACC ACCCCCCGCTTTCCCTATCTGTGCC AATACCNCATGGGA 153 B4 AGGCGCGTGCCGCTGGTTTCTGGGC GGCTGTACCCCGGAAAAAAACGATT GCTGCCAGCGCCTGTATTGCGGCCC GTTTGTGTGCGTG 154 B5 AGCCCGGTGTGCACCCCGAGCGGCC AGCCGTGTCGCGAAAACAAAGATTG CTGCAGCAAAAAATGCAAAACC ACCGGCATTGTGAAACTGTGCCGCT GG 155 B6 GCGTGCAGCAAAAAATGGGAATATT GTACCAAAGATAGCGAATGCTGCCC GCATCTGGGCTGCTGGAAACGCCGC CGCAGCTTTGAAGTGTGCGTGCCGA AAACCCCGAAAACC 156 Cl CGCTGCATTGAAGAAGGCAAATGGT GTACCAAAGATGAAGATTGCTGCAA ACATCTGGCGTGCAACCGCAAACAT AAATGGTGCAAATATAAACTGTGG 157 C2, AGCCCGACCTGCATTCGCAGCGGCC F2 AGCCGTGTGCGGATAGCGATGATTG CTGCGAAACCTTTCATTGCAAATGG GTGTTTTTTACCAGCAAATTTATGT GCCGCCGCGTGTGGGGCAAAGAT 158 C3 AGCACCTGCACCCCGACCGATCAGC CGTGTGCGGATAGCGATGATTGCTG CGAAACCTTTCATTGCAAATGGGTG TTTTTTACCAGCAAATTTATGTGCC GCCGCGTGTGGGGCAAAGAT 159 C4 AAATGCCGCTGGCTGTTTGGCGGGG TACCCCGGGCAAAAACGAATGCTGG CCGAACTATGCGTGCCATAGCTATT GGGAATGGGGCCTGTGGGATGGCAG CTTTGGATCCG 160 C5 GGCTGCAAATGGTATCTGGGCGATT GTGCGGATAGCGATGATTGCTGCGA AACCTTTCATTGCAAATGGGTGTTT TTTACCAGCAAATTTATGTGCCGCC GCGTGTGGGGCAAAGAT 161 C6, AGCAGCACCTGCATTCCGAGCGGCC D5 AGCCGTGTGCGGATAGCGATGATTG CTGCGAAACCTTTCATTGCAAA TGGGTGTTTTTTACCAGCAAATTTA TGTGCCGCCGCGTGTGGGGCAAAGA T 162 D3 GCGTGCAGCAAAAAATGGGAATATT GTAAAGAAAAACTGTGCTGCAGCGG CTATGTGTGCAAACGCCGCGGCACC AACATTGAAAAACGCTGCCGCGGA 163 D4 GCGTGCGGCCAGTTTTGGTGGAAAT GTACCAGCGATAGCGATTGCTGCCC GAACTGGGTGTGCCGCCTGTGG TGCAAATATAAACTG 164 D6, TGCCGCTATTGGCTGGGCGGCTGTA E2 GCCAGGATGGCGATTGCTGCAAACA TCTGCAGTGCAGCCCGCGCTGGGGC TGGTGCATTTATAGCACCCGCGGCG GCCGC 165 El GATTGCGGCACCATTTGGCATTATT GTACCCCGGAAAAAAACGATTGCTG CCAGCGCCTGTATTGCAGCCCGCGC TGGAGGCTGGTGCATTTA 166 E3 ATTGCGTGCGCGCCGCGCTTTAGCA TTTGTGATCCGAAAAACGATAAATG CTGCCCGAACCGCGTGTGCAGC GATAAACATAAATGGTGCAAATGGA AACTG 167 E4 AGCAGCACCTGCATTCCGAGCGGCC AGCCGTGTCGCGAAAACAAAGATTG CTGCAGCAAAAAATGCAGCGATAAA CATAAATGGTGCAAATGGAAACTGG GA 168 E5 GATGGCGAATGCGGCGGCTTTTGGT GGAAATGTAAAAACAGCAACGATTG CTGCAAAGATCTGGTGTGCAAAGAA AAATGGCCGATTACCTATAAAATTT GCGTGTGGGATCGCACCTTT 169 E6 ATTGCGTGCGCGCCGCGCTTTAGCC TGTGTGATACCAGCAAAGATTGCTG CGAAGGCTATGTGTGCAACCGC AAACATAAATGGTGCAAATATAAAC TGTGG 170 F4 GAATGCAAAGGCTTTGGCAAAAGCT GTGCGGATAGCGATGATTGCTGCGA AACCTTTCATTGCAAATGGGTGTTT TTTACCAGCAAATTTATGTGCCGCC GCGTGTGGGGCAAAGAT 171 F5 AGCCCGGTGTGCACCCCGAGCGGCC AGCCGTGTGCGGATAGCGATGATTG CTGCGAAACCTTTCATTGCAAATGG GTGTTTTTTACCAGCAAATTTATGT GCCGCCGCGTGTGGGGCAAAGAT 172 F6 GATGATTGCGGCGGCCTGTTTAGCG GCTGTACCCCGGGCAAAAACGAATG CTGCCCGAACCGCGTGTGCAAA ATTGGCCTGTATCTGTGCATTTGGA GCCCG 173 G1 GGCTGCCTGGGCGATAAATGTGCGG ATAGCGATGATTGCTGCGAAACCTT TCATTGCAAATGGGTGTTTTTTACC AGCAAATTTATGTGCCGCCGCGTGT GGGGCAAAGAT 174 G3 TGCCGCTATCTGTTTGGCGGCTGTG CGTGGTTTAGCGGCGAAAGCTGCTG CACCGGCATTTGCAGCCCGCGCTGG GGCTGGTGCATTTATAGCACCCGCG GCGGCCGC 175 G4 GGCGATTGCCTGCCGCATCTGAAAC TGTGTAACCCGAACGATGATAAATG CTGCCGCCCGAAACTGAAATGCAGC CGCCGCGGCACCAACCCGGAAAAAC GCTGCCGC 176 G6 GATGATTGCGGCACCCTGTTTAGCG GCTGTCCGTATAGCAAATATTGCTG CAGCGGCAGCTGCAAACGCCGCGGC ACCAACATTGAAAAACGCTGCCGC 177 H4 GCTGCCTGTGCGATAGATGTGTNCA TAGCGGTGATTGTTGCGAAGACTTT CATTGCACCTGCGAGTTTTTTAACA TGTAATTTATG

In some embodiments, a polypeptide component is composed of one or more polypeptide elements, each of which has an amino acid sequence that is substantially identical to a reference sequence element A, B, or C as set forth in Table 3A. In some embodiments, one or more A, B, C reference sequence elements is or comprises a wild type toxin sequence element. In some embodiments, a polypeptide component has an amino acid sequence that comprises or consists of a single sequence element corresponding to an A reference sequence element, a single sequence element corresponding to a B reference sequence element, and a single sequence element corresponding to a C reference sequence element. In some such embodiments, the single sequence elements are arranged in a linear order as follows: A-B-C. Examples of Hv1 modulating agents having A-B-C sequence elements are depicted in FIG. 2 and Table 2. Examples of nucleotide sequences encoding polypeptide sequence elements A, B, and C are set forth in Table 3B.

TABLE 3A SEQ ID  NO:  Element A 178 AACLGMFESC 179 ACGQFWWKC 180 ACKGVFDAC 181 ACREWLGGC 182 ADCGWLFHSC 183 CAAEGIPC 184 CGGWMAKC 185 CIGEGVPC 186 CMGYDIHC 187 DCAGYMREC 188 DCGTIWHYC 189 DCLGFLWKC 190 DCLGLFWIC 191 DCLGWFKGC 192 DCLGWFKSC 193 DCRALYGGC 194 DCRKMFGGC 195 DCTRMFGAC 196 DCVRFWGKC 197 DDCGGLFSGC 198 DDCGKLFSGC 199 DDCGTLFSGC 200 DDCLGMFSSC 201 DDDCGWIMDD C 202 DGECGGFWWK C 203 ECGKFMWKC 204 ECGTLFSGC 205 ECKGFGKSC 206 ECKKLFGGC 207 ECKWYLGDC 208 ECKYLWGTC 209 ECLEIFKAC 210 ECLGFGKGC 211 ECRKMFGGC 212 ECRWLFGGC 213 ECRWYLGGC 214 ECRYFWGEC 215 ECRYLFGGC 216 ECRYWLGGC 217 ECRYWLGTC 218 ECTKFLGGC 219 ECTKLLGGC 220 EDCIPKWKGC 221 EGECGGFWWK C 222 GACRWFLGGC 223 GCANAYKSC 224 GCGGLMAGC 225 GCGGLMDGC 226 GCGTMWSPC 227 GCIPSFGEC 228 GCKGFGDSC 229 GCKLTFWKC 230 GCLEFWWKC 231 GCLGDKC 232 GCNRKNKKC 233 GCQKFFWTC 234 GDCLPHLKLC 235 GDCLPHLKRC 236 GGCLPHNRFC 237 GVDKAGCRYM FGGC 238 GVDKEGCRKL LGGC 239 IACAPRFSIC 240 IACAPRFSLC 241 IACAPRGLLC 242 KCLPPGKPC 243 LCSREGEFC 244 QCGEFMWKC 245 RCIEEGKWC 246 SAVCIPSGQP C 247 SCKLTFWRC 248 SECRWFMGGC 249 SEKDCIKHLQ RC 250 SFCIPFKPC 251 SPTCIPSGQP C 252 SPTCIPTGQP C 253 SPTCIRSGQP C 254 SPVCTPSGQP C 255 SSTCIPSGQP C 256 SSTCIRTDQP C 257 STCTPTDQPC 258 SVCIPSGQPC 259 TCRYLFGGC 260 TCYDIGELC 261 VCRGYGLPC 262 YCQKWLWTC 263 YCQKWMWTC 264 CKQADEPC 265 ACRKKWEYC 266 DDDCEPPGNF C 267 VKPCRKEGQL C 268 WCKQSGEMC 269 CLSGGEVC 270 GKPCHEEGCQ L 271 CIPFLHPC 272 ACSKKWEYC Element B 273 ADSDDCCETF HC 274 AWFSGESCCT GIC 275 DEERKCCEGL VC 276 DENDPRCCSG LVC 277 DGKSTFCCSG FNC 278 DGKSTFCCSG YNC 279 DPDNDKCCEG YKC 280 DPKNDKCCKN YTC 281 DPKNDKCCPN RVC 282 DPNNDKCCPN REC 283 DPNNDKCCPN RVC 284 DPNPVKDLPC CSGLAC 285 DSARKCCEGL VC 286 DSERKCCEDM VC 287 DSERKCCEGM VC 288 DSERKCCEGY VC 289 DSKRACCEGL RC 290 DSKRKCCEDM VC 291 DSNADCCEGY VC 292 DSTLDCCKHL SC 293 DTNADCCEGY VC 294 DTSKDCCEGY VC 295 DYNNGCCSGY VC 296 EKDEHCCEHL GC 297 EKDSDCCEHL GC 298 ESNADCCENW AC 299 FRDKECCKGL TC 300 GAGKPTCCSG YDC 301 GEGKPPCCAN FAC 302 GRGKPPCCKG YAC 303 GSGKPACCPK YVC 304 GTDQSECCEG WKC 305 HPGQPPCCSG LAC 306 KADNDCCGKK C 307 KAHEDCCEHL RC 308 KEDSECCEHL QC 309 KEKLCCSGYV C 310 KENKDCCSKK C 311 KKDKECCGWN IC 312 KNKKECCGWN AC 313 KNSNDCCKDL VC 314 KSDENCCKKF KC 315 KSTSDCCEHL SC 316 KTTADCCKHL AC 37 KTTADCCKHL GC 318 KTTSDCCKHL GC 319 NALSGPRCCS GLKC 320 NDEMVCCEHL VC 321 NGPHTCCWGY NGYKKAC 322 NPDNDKCCEG RKC 323 NPNDDKCCRP KLKC 324 NPSNDKCCRP NLVC 325 NPSNDQCCKS ANLVC 326 NPSNDQCCKS SKLVC 327 NPSNDQCCKS SNLVC 328 NSDADCCRYG ERC 329 NSDKECCKGL RC 330 NYMDDKCCPG YKC 331 PKKAPCCGRL EC 332 PYHESCCSGS C 333 PYNEHCCSGS C 334 PYNENCCSKS C 335 PYNENCCSQS C 336 PYNESCCSGS C 337 PYSKYCCSGS C 338 QPNTQPCCNN AEEEQTINC 339 RENKDCCSKK C 340 RRDSDCCPHL GC 341 SAGQTCCKHL VC 342 SEDSECCPHL GC 343 SKDADCCAHL EC 344 SKHEDCCAHL AC 345 SKTGDCCSHL SC 346 SQDGDCCKHL QC 347 SQTSDCCPHL AC 348 SSDKPCCSGY YC 349 SSTSDCCKHL SC 350 STEKPCCDNF SC 351 STHADCCEGF IC 352 SVDSDCCAHL GC 353 SVHSDCCAHL GC 354 SVNDDCCPRL GC 355 TDRLPCCFGL EC 356 TIDDDCCPHL GC 357 TKDEDCCKHL AC 358 TKDSECCPHL GC 359 TPEKNDCCQR LYC 360 TPGKNECCPN RVC 361 TPGKNECCPN YAC 362 TSDSDCCPNW VC 363 TTSSECCAHL GC 364 VNRHGDCCEG LEC 365 VPGKNECCSG YAC 366 YGATQKIPCC GVC 367 YKLRKCCAGF YC 368 DVFSLDCCTG IC 369 IVPIIGFIYC CPGLIC 370 GMIKIGPPCC SGWC 371 DPIFQNCCRG WNC 372 NVLDQNCCDG YC 373 DFLFPKCCNY C 374 DPFLQNCCLG WNC 375 TFFFPDCCNS IC 376 IVPILGFVYC CPGLIC Element C 377 ALGICMPR 378 ATTGRFRYLC KYQI 379 DRRDQWCKWN PW 380 ELWCKYNL 381 ERSSPWCKID IW 382 HLWCKYK 383 HSLFSYCAWD LTFSD 384 HSNYEWCIWD GTFSK 385 HSNYEWCVWD GT 386 HSRWDWCIWD GTF 387 HSYWEWCLWD GSF 388 ICSGXNWK 389 ISTKVNYYCR PDRGP 390 KAFVLHCYRN 391 KDVLYYCAWD GTF 392 KEKWPITYKI CVWDRTF 393 KELSIWDSRC L 394 KFRDKYCAWD FTFS 395 KGPSPKQKKC TRP 396 KGRFVNTWPT FCLV 397 KIGLYLCIWS P 398 KLWCRKIIG 399 KLWCRYERTW 400 KMGLDYCAWD GTF 401 KMGLYYCAWD GTF 402 KPTLKYCAWD GT 403 KPTLKYCAWD GTF 404 KPTSKYCAWD GTI 405 KQKWPFYCAW DWSF 406 KRRGTNAEKR CR 407 KRRGTNIEKR CR 408 KRTFNYCAWD GSFSK 409 KSKWPRNICV WDGSV 410 KTTGIVKLCR W 411 KWVFFTSKFM CRRVWGKD 412 LKPTLHGIWY KHHYCYTQ 413 LKPTLHGIWY KSYYCYKK 414 NGNTVYRCA 415 NKKHGWCGWD GTF 416 NKKYWHCGWD GTF 417 NRKHKWCKYK LW 418 NRRDKWCKYK LW 419 NSRDKWCKVL L 420 QLWCKKRL 421 QPAIKWCIWS P 422 QSRIANMWPT FCLV 423 QSRIANMWPT FCSQ 424 RKKWPYHCGW DGTF 425 RKKWPYHCVW DWTV 426 RLWCKKII 427 RLWCKKKIEE G 428 RLWCKKKIEW 429 RLWCKKKLW 430 RLWCKKRL 431 RLWCKLDW 432 RLWCKRIINM 433 RLWCKYKL 434 RRAKPSWCGW DFTF 435 RRAKPSWCGW DFTV 436 RRTLPTYCAW DLTFP 437 RSDGKYCAWD GTF 438 RSDWKYCAWD GTFS 439 RSRDQWCKYK LW 440 RVRDQWCKYK LW 441 SDKHKWCKWK L 442 SHNKCT 443 SKLFKLCNFS F 444 SKTGFVKNIC KYEM 445 SKTWGWCAVE AP 446 SPKHGWCVWD WTFRK 447 SPKWGLCNFP MP 448 SPRWGWCIYS TRGGR 449 SPTWKWCVLK SPGRR 450 SPTWKWCVYA RP 451 SQHRLCSVKA 452 SRKDKWCKYQ I 453 SRKHRWCKYE I 454 SRKTRWCKYQ I 455 SRQLCKYVID W 456 SRRDRWCKYD L 457 SRRDRWCKYY L 458 SRRGTNPEKR CR 459 SRRHGWCVWD GTFS 460 SRTWKWCVLA GPW 461 SSKHKWCKVY L 462 SSRWKWCVLA SPF 463 SSRWKWCVLP APW 464 TFKENENGNT VKRCD 465 TFKTNENGNT VKRCD 466 TGLCIPP 467 TRFNVCGK 468 TWPTEICID 469 TYKANENGNQ VKRCD 470 TYKENENGNT VKRCD 471 TYKENENGNT VQRCD 472 TYKTNENGNS VQRCD 473 VKTSGYWWYK KTYCRRKS 474 WKRRRSFEVC VPKTPKT 475 LGVCMW 476 FFACA 477 VLFCV 478 IVFVCT 479 ILLFCS 480 VFVCI 481 AQFICL 482 GPFVCV

TABLE 3B SEQ ID NO. Element A 483 GCGGCGTGCCTGG GCATGTTTGAAAGC TGT 484 GCGTGCGGCCAGT TTTGGTGGAAATGT 485 GCGTGCAAAGGCG TGTTTGATGCGTGT 486 GCGTGCCGCGAAT GGCTGGGCGGCTG T 487 GCGGATTGCGGCT GGCTGTTTCATAGC TGT 488 TGCGCGGCGGAAG GCATTCCGTGT 489 TGCGGCGGCTGGA TGGCGAAATGT 490 TGCATTGGCGAAGG CGTGCCGTGT 491 TGCATGGGCTATGA TATTCATTGT 492 GATTGCGCGGGCT ATATGCGCGAATGT 493 GATTGCGGCACCAT TTGGCATTATTGT GATTGCCTGGGCTT 494 TCTGTGGAAATGT 495 GATTGCCTGGGCCT GTTTTGGATTGT 496 GATTGCCTGGGCTG GTTTAAAGGCTGT 497 GATTGCCTGGGCTG GTTTAAAAGCTGT 498 GATTGCCGCGCGC TGTATGGCGGCTGT 499 GATTGCCGCAAAAT GTTTGGCGGCTGT 500 GATTGCACCCGCAT GTTTGGCGCGTGT 501 GATTGCGTGCGCTT TTGGGGCAAATGT 502 GATGATTGCGGCG GCCTGTTTAGCGGC TGT 503 GATGATTGCGGCAA ACTGTTTAGCGGCT GT 504 GATGATTGCGGCAC CCTGTTTAGCGGCT GT 505 GATGATTGCCTGGG CATGTTTAGCAGCT GT 506 GATGATGATTGCGG CTGGATTATGGATG ATTGT 507 GATGGCGAATGCG GCGGCTTTTGGTGG AAATGT 508 GAATGCGGCAAATT TATGTGGAAATGT 509 GAATGCGGCACCCT GTTTAGCGGCTGT 510 GAATGCAAAGGCTT TGGCAAAAGCTGT 511 GAATGCAAAAAACT GTTTGGCGGCTGT 512 GAATGCAAATGGTA TCTGGGCGATTGT 513 GAATGCAAATATCT GTGGGGCACCTGT 514 GAATGCCTGGAAAT TTTTAAAGCGTGT 515 GAATGCCTGGGCTT TGGCAAAGGCTGT 516 GAATGCCGCAAAAT GTTTGGCGGCTGT 517 GAATGCCGCTGGCT GTTTGGCGGTGT 518 GAATGCCGCTGGTA TCTGGGCGGCTGT 519 GAATGCCGCTATTT TTGGGGCGAATGT 520 GAATGCCGCTATCT GTTTGGCGGCTGT 521 GAATGCCGCTATTG GCTGGGCGGCTGT 522 GAATGCCGCTATTG GCTGGGCACCTGT 523 GAATGCACCAAATT TCTGGGCGGCTGT 524 GAATGCACCAAACT GCTGGGCGGCTGT 525 GAAGATTGCATTCC GAAATGGAAAGGCT GT 526 GAAGGCGAATGCG GCGGCTTTTGGTGG AAATGT 527 GGCGCGTGCCGCT GGTTTCTGGGCGG CTGT 528 GGCTGCGCGAACG CGTATAAAAGCTGT 529 GGCTGCGGCGGCC TGATGGCGGGCTG T 530 GGCTGCGGCGGCC TGATGGATGGCTGT 531 GGCTGCGGCACCA TGTGGAGCCCGTGT 532 GGCTGCATTCCGAG CTTTGGCGAATGT 533 GGCTGCAAAGGCTT TGGCGATAGCTGT 534 GGCTGCAAACTGAC CTTTTGGAAATGT 535 GGCTGCCTGGAATT TTGGTGGAAATGT 536 GGCTGCCTGGGCG ATAAATGT 537 GGCTGCAACCGCA AAAACAAAAAATGT 538 GGCTGCCAGAAATT TTTTTGGACCTGT 539 GGCGATTGCCTGC CGCATCTGAAACTG TGT 540 GGCGATTGCCTGC CGCATCTGAAACGC TGT 541 GGCGGCTGCCTGC CGCATAACCGCTTT TGT 542 GGCGTGGATAAAG CGGGCTGCCGCTA TATGTTTGGCGGCT GT 543 GGCGTGGATAAAGA AGGCTGCCGCAAA CTGCTGGGCGGCT GT 544 ATTGCGTGCGCGC CGCGCTTTAGCATT TGT 545 ATTGCGTGCGCGC CGCGCTTTAGCCTG TGT 546 ATTGCGTGCGCGC CGCGCGGCCTGCT GTGT 547 AAATGCCTGCCGCC GGGCAAACCGTGT 548 CTGTGCAGCCGCG AAGGCGAATTT 549 CAGTGCGGCGAATT TATGTGGAAATGT 550 CGCTGCATTGAAGA AGGCAAATGGTGT 551 AGCGCGGTGTGCA TTCCGAGCGGCCA GCCGTGT 552 AGCTGCAAACTGAC CTTTTGGCGCTGT 553 AGCGAATGCCGCT GGTTTATGGGCGG CTGT 554 AGCGAAAAAGATTG CATTAAACATCTGC AGCGCTGT 555 AGCTTTTGCATTCC GTTTAAACCGTGT 556 AGCCCGACCTGCAT TCCGAGCGGCCAG CCGTGT 557 AGCCCGACCTGCAT TCCGACCGGCCAG CCGTGT 558 AGCCCGACCTGCAT TCGCAGCGGCCAG CCGTGT 559 AGCCCGGTGTGCA CCCCGAGCGGCCA GCCGTGT 560 AGCAGCACCTGCAT TCCGAGCGGCCAG CCGTGT 561 CGGCTGGCCGCTC GGAATGCAGGTGCT GCTTGT 562 AGCACCTGCACCCC GACCGATCAGCCGT GT 563 AGCGTGTGCATTCC GAGCGGCCAGCCG TGT 564 ACCTGCCGCTATCT GTTTGGCGGCTGT 565 ACCTGCTATGATAT TGGCGAACTGTGT 566 GTGTGCCGCGGCT ATGGCCTGCCGTGT 567 TATTGCCAGAAATG GCTGTGGACCTGT 568 TATTGCCAGAAATG GATGTGGACCTGT 569 TGCAAACAGGCGG ATGAACCGTGT 570 GCGTGCCGCAAAAA ATGGGAATATTGT 571 GATGATGATTGCGA ACCGCCGGGCAAC TTTTGT 572 GTGAAACCGTGCC GCAAAGAAGGCCA GCTGTGT 573 TGGTGCAAACAGAG CGGCGAAATGTGT 574 TGCCTGAGCGGCG GCGAAGTGTGT 575 GGCAAACCGTGCC ATGAAGAAGGCCAG CTGTGT 576 TGCATTCCGTTTCT GCATCCGTGT 577 GCGTGCAGCAAAAA ATGGGAATATTGT Element B 578 GCGGATAGCGATGATTGCTGC GAAACCTTTCATTGC 579 GCGTGGTTTAGCGGCGAAAGC TGCTGCACCGGCATTTGC 580 GATGAAGAACGCAAATGCTGC GAAGGCCTGGTGTGC 581 GATGAAAACGATCCGCGCTGC TGCAGCGGCCTGGTGTGC 582 GATGGCAAAAGCACCTTTTGCT GCAGCGGCTTTAACTGC 583 GATGGCAAAAGCACCTTTTGCT GCAGCGGCTATAACTGC 584 GATCCGGATAACGATAAATGCT GCGAAGGCTATAAATGC 585 GATCCGAAAAACGATAAATGCT GCAAAAACTATACCTGC 586 GATCCGAAAAACGATAAATGCT GCCCGAACCGCGTGTGC 587 GATCCGAACAACGATAAATGCT GCCCGAACCGCGAATGC 588 GATCCGAACAACGATAAATGCT GCCCGAACCGCGTGTGC GATCCGAACCCGGTGAAAGAT 589 CTGCCGTGCTGCAGCGGCCTG GCGTGC GATAGCGCGCGCAAATGCTGC 590 GAAGGCCTGGTGTGC 591 GATAGCGAACGCAAATGCTGC GAAGATATGGTGTGC 592 GATAGCGAACGCAAATGCTGC GAAGGCATGGTGTGC 593 GATAGCGAACGCAAATGCTGC GAAGGCTATGTGTGC 594 GATAGCAAACGCGCGTGCTGC GAAGGCCTGCGCTGC 595 GATAGCAAACGCAAATGCTGC GAAGATATGGTGTGC 596 GATAGCAACGCGGATTGCTGC GAAGGCTATGTGTGC 597 GATAGCACCCTGGATTGCTGC AAACATCTGAGCTGC 598 GATACCAACGCGGATTGCTGC GAAGGCTATGTGTGC 599 GATACCAGCAAAGATTGCTGC GAAGGCTATGTGTGC 600 GATTATAACAACGGCTGCTGCA GCGGCTATGTGTGC 601 GAAAAAGATGAACATTGCTGCG AACATCTGGGCTGC 602 GAAAAAGATAGCGATTGCTGC GAACATCTGGGCTGC 603 GAAAGCAACGCGGATTGCTGC GAAAACTGGGCGTGC 604 TTTCGCGATAAAGAATGCTGCA AAGGCCTGACCTGC 605 GGCGCGGGCAAACCGACCTGC TGCAGCGGCTATGATTGC 606 GGCGAAGGCAAACCGCCGTGC TGCGCGAACTTTGCGTGC 607 GGCCGCGGCAAACCGCCGTGC TGCAAAGGCTATGCGTGC 608 GGCAGCGGCAAACCGGCGTGC TGCCCGAAATATGTGTGC 609 GGCACCGATCAGAGCGAATGC TGCGAAGGCTGGAAATGC 610 CATCCGGGCCAGCCGCCGTGC TGCAGCGGCCTGGCGTGC 611 AAAGCGGATAACGATTGCTGC GGCAAAAAATGC 612 AAAGCGCATGAAGATTGCTGC GAACATCTGCGCTGC 613 AAAGAAGATAGCGAATGCTGC GAACATCTGCAGTGC 614 AAAGAAAAACTGTGCTGCAGC GGCTATGTGTGC 615 AAAGAAAACAAAGATTGCTGCA GCAAAAAATGC 616 AAAAAAGATAAAGAATGCTGCG GCTGGAACATTTGC 617 AAAAACAAAAAAGAATGCTGCG GCTGGAACGCGTGC 618 AAAAACAGCAACGATTGCTGCA AAGATCTGGTGTGC 619 AAAAGCGATGAAAACTGCTGCA AAAAATTTAAATGC 620 AAAAGCACCAGCGATTGCTGC GAACATCTGAGCTGC 621 AAAACCACCGCGGATTGCTGC AAACATCTGGCGTGC 622 AAAACCACCGCGGATTGCTGC AAACATCTGGGCTGC 623 AAAACCACCAGCGATTGCTGCA AACATCTGGGCTGC 624 AACGCGCTGAGCGGCCCGCGC TGCTGCAGCGGCCTGAAATGC 625 AACGATGAAATGGTGTGCTGC GAACATCTGGTGTGC 626 AACGGCCCGCATACCTGCTGC TGGGGCTATAACGGCTATAAAA AAGCGTGC 627 AACCCGGATAACGATAAATGCT GCGAAGGCCGCAAATGC 628 AACCCGAACGATGATAAATGCT GCCGCCCGAAACTGAAATGC 629 AACCCGAGCAACGATAAATGCT GCCGCCCGAACCTGGTGTGC 630 AACCCGAGCAACGATCAGTGC TGCAAAAGCGCGAACCTGGTG TGC 631 AACCCGAGCAACGATCAGTGC TGCAAAAGCAGCAAACTGGTGT GC 632 AACCCGAGCAACGATCAGTGC TGCAAAAGCAGCAACCTGGTG TGC 633 AACAGCGATGCGGATTGCTGC CGCTATGGCGAACGCTGC 634 AACAGCGATAAAGAATGCTGCA AAGGCCTGCGCTGC 635 AACTATATGGATGATAAATGCT GCCCGGGCTATAAATGC 636 CCGAAAAAAGCGCCGTGCTGC GGCCGCCTGGAATGC 637 CCGTATCATGAAAGCTGCTGCA GCGGCAGCTGC 638 CCGTATAACGAACATTGCTGCA GCGGCAGCTGC 639 CCGTATAACGAAAACTGCTGCA GCAAAAGCTGC 640 CCGTATAACGAAAACTGCTGCA GCCAGAGCTGC 641 CCGTATAACGAAAGCTGCTGCA GCGGCAGCTGC 642 CCGTATAGCAAATATTGCTGCA GCGGCAGCTGC 643 CAGCCGAACACCCAGCCGTGC TGCAACAACGCGGAAGAAGAA CAGACCATTAACTGC 644 CGCGAAAACAAAGATTGCTGCA GCAAAAAATGC 645 CGCCGCGATAGCGATTGCTGC CCGCATCTGGGCTGC 646 AGCGCGGGCCAGACCTGCTGC AAACATCTGGTGTGC 647 AGCGAAGATAGCGAATGCTGC CCGCATCTGGGCTGC 648 AGCAAAGATGCGGATTGCTGC GCGCATCTGGAATGC 649 AGCAAACATGAAGATTGCTGCG CGCATCTGGCGTGC 650 AGCAAAACCGGCGATTGCTGC AGCCATCTGAGCTGC 651 AGCCAGGATGGCGATTGCTGC AAACATCTGCAGTGC 652 AGCCAGACCAGCGATTGCTGC CCGCATCTGGCGTGC 653 AGCAGCGATAAACCGTGCTGC AGCGGCTATTATTGC 654 AGCAGCACCAGCGATTGCTGC AAACATCTGAGCTGC 655 AGCACCGAAAAACCGTGCTGC GATAACTTTAGCTGC 656 AGCACCCATGCGGATTGCTGC GAAGGCTTTATTTGC 657 AGCGTGGATAGCGATTGCTGC GCGCATCTGGGCTGC 658 AGCGTGCATAGCGATTGCTGC GCGCATCTGGGCTGC 659 AGCGTGAACGATGATTGCTGC CCGCGCCTGGGCTGC 660 ACCGATCGCCTGCCGTGCTGC TTTGGCCTGGAATGC 661 ACCATTGATGATGATTGCTGCC CGCATCTGGGCTGC 662 ACCAAAGATGAAGATTGCTGCA AACATCTGGCGTGC 663 ACCAAAGATAGCGAATGCTGC CCGCATCTGGGCTGC 664 ACCCCGGAAAAAAACGATTGCT GCCAGCGCCTGTATTGC 665 ACCCCGGGCAAAAACGAATGC TGCCCGAACCGCGTGTGC 666 ACCCCGGGCAAAAACGAATGC TGCCCGAACTATGCGTGC 667 ACCAGCGATAGCGATTGCTGC CCGAACTGGGTGTGC 668 ACCACCAGCAGCGAATGCTGC GCGCATCTGGGCTGC 669 GTGAACCGCCATGGCGATTGC TGCGAAGGCCTGGAATGC 670 GTGCCGGGCAAAAACGAATGC TGCAGCGGCTATGCGTGC 671 TATGGCGCGACCCAGAAAATTC CGTGCTGCGGCGTGTGC 672 TATAAACTGCGCAAATGCTGCG CGGGCTTTTATTGC 673 GATGTGTTTAGCCTGGATTGCT GCACCGGCATTTGC 674 ATTGTGCCGATTATTGGCTTTA TTTATTGCTGCCCGGGCCTGAT TTGC 675 GGCATGATTAAAATTGGCCCGC CGTGCTGCAGCGGCTGGTGC 676 GATCCGATTTTTCAGAACTGCT GCCGCGGCTGGAACTGC 677 AACGTGCTGGATCAGAACTGCT GCGATGGCTATTGC 678 GATTTTCTGTTTCCGAAATGCT GCAACTATTGC 679 GATCCGTTTCTGCAGAACTGCT GCCTGGGCTGGAACTGC 680 ACCTTTTTTTTTCCGGATTGCT GCAACAGCATTTGC 681 ATTGTGCCGATTCTGGGCTTTG TGTATTGCTGCCCGGGCCTGA TTTGC Element C 682 GCGCTGGGCATTTGCAT GCCGCGC 683 GCGACCACCGGCCGCTT TCGCTATCTGTGCAAATA TCAGATT 684 GATCGCCGCGATCAGTG GTGCAAATGGAACCCGT GG 685 GAACTGTGGTGCAAATA TAACCTG 686 GAACGCAGCAGCCCGTG GTGCAAAATTGATATTTG G 687 CATCTGTGGTGCAAATAT AAA 688 CATAGCCTGTTTAGCTAT TGCGCGTGGGATCTGAC CTTTAGCGAT 689 CATAGCAACTATGAATG GTGCATTTGGGATGGCA CCTTTAGCAAA 690 CATAGCAACTATGAATG GTGCGTGTGGGATGGCA CC 691 CATAGCCGCTGGGATTG GTGCATTTGGGATGGCA CCTTT 692 CATAGCTATTGGGAATG GTGCCTGTGGGATGGCA GCTTT 693 ATTTGCAGCGGCAACTG GAAA 694 ATTAGCACCAAAGTGAA CTATTATCGCCCGGATC GCGGCCCG 695 AAAGCGTTTGTGCTGCA TTGCTATCGCAAC 696 AAAGATGTGCTGTATTAT TGCGCGTGGGATGGCAC CTTT 697 AAAGAAAAATGGCCGAT TACCTATAAAATTTGCGT GTGGGATCGCACCTTT 698 AAAGAACTGAGCATTTG GGATAGCCGCTGCCTG 699 AAATTTCGCGATAAATAT TGCGCGTGGGATTTTAC CTTTAGC 700 AAAGGCCCGAGCCCGAA ACAGAAAAAATGCACCC GCCCG 701 AAAGGCCGCTTTGTGAA CACCTGGCCGACCTTTT GCCTGGTG 702 AAAATTGGCCTGTATCTG TGCATTTGGAGCCCG 703 AAACTGTGGTGCCGCAA AATTATTGGC 704 AAACTGTGGTGCCGCTA TGAACGCACCTGG 705 AAAATGGGCCTGGATTA TTGCGCGTGGGATGGCA CCTTT 706 AAAATGGGCCTGTATTAT TGCGCGTGGGATGGCAC CTTT 707 AAACCGACCCTGAAATAT TGCGCGTGGGATGGCAC C 708 AAACCGACCCTGAAATAT TGCGCGTGGGATGGCAC CTTT 709 AAACCGACCAGCAAATA TTGCGCGTGGGATGGCA CCATT 710 AAACAGAAATGGCCGTT TTATTGCGCGTGGGATT GGAGCTTT 711 AAACGCCGCGGCACCAA CGCGGAAAAACGCTGCC GC 712 AAACGCCGCGGCACCAA CATTGAAAAACGCTGCC GC 713 AAACGCACCTTTAACTAT TGCGCGTGGGATGGCAG CTTTAGCAAA 714 AAAAGCAAATGGCCGCG CAACATTTGCGTGTGGG ATGGCAGCGTG 715 AAAACCACCGGCATTGT GAAACTGTGCCGCTGG 716 AAATGGGTGTTTTTTACC AGCAAATTTATGTGCCG CCGCGTGTGGGGCAAAG AT 717 CTGAAACCGACCCTGCA TGGCATTTGGTATAAACA TCATTATTGCTATACCCA G 718 CTGAAACCGACCCTGCA TGGCATTTGGTATAAAAG CTATTATTGCTATAAAAA A 719 AACGGCAACACCGTGTA TCGCTGCGCG 720 AACAAAAAACATGGCTG GTGCGGCTGGGATGGCA CCTTT 721 AACAAAAAATATTGGCAT TGCGGCTGGGATGGCAC CTTT 722 AACCGCAAACATAAATG GTGCAAATATAAACTGTG G 723 AACCGCCGCGATAAATG GTGCAAATATAAACTGTG G 724 AACAGCCGCGATAAATG GTGCAAAGTGCTGCTG 725 CAGCTGTGGTGCAAAAA ACGCCTG 726 CAGCCGGCGATTAAATG GTGCATTTGGAGCCCG 727 CAGAGCCGCATTGCGAA CATGTGGCCGACCTTTT GCCTGGTG 728 CAGAGCCGCATTGCGAA CATGTGGCCGACCTTTT GCAGCCAG 729 CGCAAAAAATGGCCGTA TCATTGCGGCTGGGATG GCACCTTT 730 CGCAAAAAATGGCCGTA TCATTGCGTGTGGGATT GGACCGTG 731 CGCCTGTGGTGCAAAAA AATTATT 732 CGCCTGTGGTGCAAAAA AAAAATTGAAGAAGGC 733 CGCCTGTGGTGCAAAAA AAAAATTGAATGG CGCCTGTGGTGCAAAAA 734 AAAACTGTGG 735 CGCCTGTGGTGCAAAAA ACGCCTG 736 CGCCTGTGGTGCAAACT GGATTGG 737 CGCCTGTGGTGCAAACG CATTATTAACATG 738 CGCCTGTGGTGCAAATA TAAACTG 739 CGCCGCGCGAAACCGA GCTGGTGCGGCTGGGAT TTTACCTTT 740 CGCCGCGCGAAACCGA GCTGGTGCGGCTGGGAT TTTACCGTG 741 CGCCGCACCCTGCCGAC CTATTGCGCGTGGGATC TGACCTTTCCG 742 CGCAGCGATGGCAAATA TTGCGCGTGGGATGGCA CCTTT 743 CGCAGCGATTGGAAATA TTGCGCGTGGGATGGCA CCTTTAGC 744 CGCAGCCGCGATCAGTG GTGCAAATATAAACTGTG G 745 CGCGTGCGCGATCAGTG GTGCAAATATAAACTGTG G 746 AGCGATAAACATAAATG GTGCAAATGGAAACTG 747 AGCCATAACAAATGCAC C 748 AGCAAACTGTTTAAACTG TGCAACTTTAGCTTT 749 AGCAAAACCGGCTTTGT GAAAAACATTTGCAAATA TGAAATG 750 AGCAAAACCTGGGGCTG GTGCGCGGTGGAAGCG CCG 751 AGCCCGAAACATGGCTG GTGCGTGTGGGATTGGA CCTTTCGCAAA 752 AGCCCGAAATGGGGCCT GTGCAACTTTCCGATGC CG 753 AGCCCGCGCTGGGGCT GGTGCATTTATAGCACC CGCGGCGGCCGC 754 AGCCCGACCTGGAAATG GTGCGTGCTGAAAAGCC CGGGCCGCCGC 755 AGCCCGACCTGGAAATG GTGCGTGTATGCGCGCC CG 756 AGCCAGCATCGCCTGTG CAGCGTGAAAGCG 757 AGCCGCAAAGATAAATG GTGCAAATATCAGATT 758 AGCCGCAAACATCGCTG GTGCAAATATGAAATT 759 AGCCGCAAAACCCGCTG GTGCAAATATCAGATT 760 AGCCGCCAGCTGTGCAA ATATGTGATTGATTGG 761 AGCCGCCGCGATCGCTG GTGCAAATATGATCTG 762 AGCCGCCGCGATCGCTG GTGCAAATATTATCTG 763 AGCCGCCGCGGCACCAA CCCGGAAAAACGCTGCC GC 764 AGCCGCCGCCATGGCTG GTGCGTGTGGGATGGCA CCTTTAGC 765 AGCCGCACCTGGAAATG GTGCGTGCTGGCGGGC CCGTGG 766 AGCAGCAAACATAAATG GTGCAAAGTGTATCTG 767 AGCAGCCGCTGGAAATG GTGCGTGCTGGCGAGCC CGTTT 768 AGCAGCCGCTGGAAATG GTGCGTGCTGCCGGCG CCGTGG 769 ACCTTTAAAGAAAACGAA AACGGCAACACCGTGAA ACGCTGCGAT 770 ACCTTTAAAACCAACGAA AACGGCAACACCGTGAA ACGCTGCGAT 771 ACCGGCCTGTGCATTCC GCCG 772 ACCCGCTTTAACGTGTG CGGCAAA 773 ACCTGGCCGACCGAAAT TTGCATTGAT 774 ACCTATAAAGCGAACGA AAACGGCAACCAGGTGA AACGCTGCGAT 775 ACCTATAAAGAAAACGAA AACGGCAACACCGTGAA ACGCTGCGAT 776 ACCTATAAAGAAAACGAA AACGGCAACACCGTGCA GCGCTGCGAT 777 ACCTATAAAACCAACGAA AACGGCAACAGCGTGCA GCGCTGCGAT 778 GTGAAAACCAGCGGCTA TTGGTGGTATAAAAAAAC CTATTGCCGCCGCAAAA GC 779 TGGAAACGCCGCCGCAG CTTTGAAGTGTGCGTGC CGAAAACCCCGAAAACC 780 CTGGGCGTGTGCATGTG G 781 TTTTTTGCGTGCGCG 782 GTGCTGTTTTGCGTG 783 ATTGTGTTTGTGTGCACC 784 ATTCTGCTGTTTTGCAGC 785 GTGTTTGTGTGCATT 786 GCGCAGTTTATTTGCCT G 787 GGCCCGTTTGTGTGCGT G

In some embodiments, reference sequence element A has an amino acid sequence GCKWYLGDC (SEQ ID NO: 809). In some embodiments, reference sequence element A has an amino acid sequence SSTCIPSGQPC (SEQ ID NO: 255). In some embodiments, reference sequence element B has an amino acid sequence ADSDDCCETFHC (SEQ ID NO: 273). In some embodiments, reference sequence element C has an amino acid sequence KWVFFTSKFMCRRVWGKD (SEQ ID NO: 411).

In some embodiments, a provided polypeptide component has an amino acid sequence that is or comprises GCKWYLGDCADSDDCCETFHCKWVFFTSKFMCRRVWGKD (SEQ ID NO: 128), as is found in the Hv1 modulating agent labeled as “C5” in Table 2A.

In some embodiments, a provided polypeptide component has an amino acid sequence that is or comprises SSTCIPSGQPCADSDDCCETFHCKWVFFTSKFMCRRVWGKD (SEQ ID NO: 129), as is found in the Hv1 modulating agent labeled as “C6” in Table 2A.

In some embodiments, a polypeptide component has an amino acid sequence that includes one or more cysteine residues at positions corresponding to those at which a cysteine residue is found in a relevant wild-type toxin (e.g., wild-type voltage sensor toxin) sequence or reference sequence element (e.g., as depicted in FIG. 2). In some embodiments, a polypeptide component has an amino acid sequence that includes all cysteine residues at positions corresponding to those at which cysteine residues are found in a relevant wild-type toxin sequence or reference sequence element. In some embodiments, a polypeptide component has an amino acid sequence that shares the same approximate relative position of cysteines (e.g., number of residues between them) with a relevant wild-type toxin sequence or reference sequence element.

In some embodiments, a polypeptide component has an amino acid sequence that includes one or more sequence elements that are identical to or includes not more than 1, 2, 3, 4, or 5 sequence differences relative to a wild-type toxin sequence element or reference sequence element.

In some embodiments, such sequence difference(s) are or comprise one or more insertions, deletions, substitutions, rearrangements (e.g., inversions) or combinations thereof. In some embodiments, such sequence difference(s) do not include any insertions. In some embodiments, such sequence difference(s) do not include any deletions. In some embodiments, such sequence differences do not include any rearrangements (e.g., inversions). In some embodiments, such sequence difference(s) may include one or more random sequence alterations.

In some embodiments, a polypeptide component has an amino acid sequence that includes one or more sequence elements that shares one or more cysteines with a sequence set forth in Table 1, Table 2, and/or Table 3. In some embodiments, such a sequence element has an amino acid sequence that shares all cysteines with a sequence set forth in Table 1, Table 2, and/or Table 3. In some embodiments, a sequence element shares the same approximate relative position of cysteines (e.g., number of residues between them) with a sequence set forth in Table 1, Table 2, and/or Table 3.

In some embodiments, a reference sequence element has an amino acid sequence of an element found in a wild-type voltage toxin sequence that differs at residues that undergo posttranslational modifications.

In some embodiments, a polypeptide component of an Hv1 modulating agent may include one or more pendant groups or other modifications, e.g., modifying or attached to one or more amino acid residues (e.g., to one or more amino acid side chains), at the polypeptide component's N-terminus, at the polypeptide component's C-terminus, or any combination thereof. In some embodiments, such pendant groups or modifications may be selected from the group consisting of acetylation, amidation, glycosylation, lipidation, methylation, pegylation, phosphorylation, etc., and combinations thereof.

In some embodiments, exemplary Hv1 modulating agents comprise a polypeptide component whose amino acid sequence further comprises one or more tag elements (e.g., a detectable tag, a localizing tag, etc).

In some embodiments, an Hv1 modulating agent may be a dimer or multimer of relevant entities (e.g., of a polypeptide component as described herein); in some embodiments, an Hv1 modulating agent may be or comprise heterodimer or heteromultimer. In some embodiments, an Hv1 modulating agent may be or comprise a homodimer or homomultimer. Exemplary Hv1 modulating agent dimers are presented in Table 4.

TABLE 4A Dimer Sequences (with linkers) SEQ ID NO: Name Sequence 788 HaTx-C6 ECRYLEGGCKTTSDCCKHLGCKFR DKYCAWDETFSGNGNGNGSSTCIP SGQPCADSDDCCETFHCKWVFFTS KFMCRRVWGKD 789 C6-C6 SSTCIPSGQPCADSDDCCETFHCK with WVFFTSKFMCRRVWGKDDSSPYVP DkTx linker VTTSSTCIPSGQPCADSDDCCETF HCKWVFFTSKFMCRRVWGKD 790 C6-C6 SSICIPSGQPCADSDDCCETFHCK with WVFFTSKFMCRRVWGKDDSSGNGN flexible GNGSSTCIPSWPCADSDDCCETFE linker ICKWVFFTSKFMCRRVWGKD 791 C6-C6 SSTCIPSGQPCADSDDCCETFHCK with WVFFTSKFMCRRVWGKDDSSGGNG long NGNGNGNGNGNGAAAGGNGNGNGN flexible GNGNGNGSSTCIPSGQPCADSDDC linker CETFHCKWVFFTSKFMCRRVWGKD

TABLE 4B Monomer C6 + signal AND dimer + signal SEQ ID NO: Name Sequence 792 C6 with signal MSALLILALVGAAVA peptide SSTCIPSGQPCADSD (MSALLILALVGAAVA) DCCETFHCKWVFFTS KFMCRRVWGKD 793 HaTx-C6 MSALLILALVGAAVA ECRYLFGGCKTTSDC CKHLGCKFRDKYCAW DFTFSGNGNGNGSST CIPSGQPCADSDDCC ETFHCKWVFFTSKFM CRRVWGKD 794 C6-C6 with DkTx MSALLILALVGAAVA linker with signal SSTCIPSGQPCADSD peptide DCCETFHCKWVFFTS KFMCRRVWGKDDSSP YVPVTTSSTCIPSGQ PCADSDDCCETFHCK WVFFTSKFMCRRVWG KD 795 C6-C6 with MSALLILALVGAAVA flexible linker SSTCIPSGQPCADSD with signal DCCETFHCKWVFFTS peptide KFMCRRVWGKDDSSG NGNGNGSSTCIPSGQ PCADSDDCCETFHCK WVFFTSKFMCRRVWG KD 796 C6-C6 with long MSALLILALVGAAVA flexible linker SSTCIPSGQPCADSD with signal DCCETFHCKWVFFTS peptide KFMCRRVWGKDDSSG GNGNGNGNGNGNGNG AAAGGNGNGNGNGNG NGNGSSTCIPSGQPC ADSDDCCETFHCKWV FFTSKFMCRRVWGKD

TABLE 4C Monomer + Mye tag, dimer + Myc tag, either/both plus signal and tag SEQ ID NO: Name Sequence 797 C6 with signal MSALLILALVGAAVA peptide and SSTCIPSGQPCADSD Myc tag DCCETFHCKWVFFTS KFMCRRV WGKDGEQKLISEEDL 798 HaTx-C6 with MSALLILALVGAAVA signal peptide ECRYLFGGCKTTSDC and Myc tag CKHLGCKFRDKYCAW DFTFSGN GNGNGSSTCIPSGQP CADSDDCCETFHCKW VFFTSKFMCRRVWGK DGEQKLI SEEDL 799 C6-C6 with MSALLILALVGAAVA DkTx linker SSTCIPSGQPCADSD with signal DCCETFHCKWVFFTS peptide and KFMCRRV Myc tag WGKDDSSPYVPVTTS STCIPSGQPCADSDD CCETFHCKWVFFTSK FMCRRVW GKDGEQKLISEEDL 800 C6-C6 with MSALLILALVGAAVA flexible SSTCIPSGQPCADSD linker with DCCETFHCKWVFFTS signal peptide KFMCRRV and Myc tag WGKDDSSGNGNGNGS STCIPSGQPCADSDD CCETFHCKWVFFTSK FMCRRVW GKDGEQKLISEEDL 801 C6-C6 with MSALLILALVGAAVA long flexible SSTCIPSGQPCADSD DCCETFHCKWVFFTS KFMCRRV WGKDDSSGGNGNGNG NGNGNGNGAAAGGNG NGNGNGNGNGNGSST CIPSGQP

TABLE 4D Monomer + GPI targeting, dimer + GPI targeting, either/both plus signal, tag and linker SEQ ID NO: Name Sequence 802 C6 with signal MSALLILALVGAAVASSTCIPSGQ peptide and Myc PCADSDDCCETFHCKWVFFTSKFM tag and GPI CRRVWGKDGEQKLISEEDLGALCN anchor GAGFATPVTLALVPALLATFWSLL 803 HaTx-C6 with MSALLILALVGAAVAECRYLFGGC signal peptide KTTSDCCKHLGCKFRDKYCAWDFT and Myc tag and FSGNGNGNGSSTCIPSGQPCADSD GPI anchor DCCETFHCKWVFFTSKFMCRRVWG KDGEQKLISEEDLGALCNGAGFAT PVTLALVPALLATFWSLL 804 C6-C6 with DkTx MSALLILALVGAAVASSTCIPSGQ linker with PCADSDDCCETFHCKWVFFTSKFM signal peptide CRRVWGKDDSSPYVPVTTSSTCIP and Myc tag and SGQPCADSDDCCETFHCKWVFFTS GPI anchor KFMCRRVWGKDGEQKLISEEDLGA LCNGAGFATPVTLALVPALLATFW SLL 805 C6-C6 with MSALLILALVGAAVASSTCIPSGQ flexible linker PCADSDDCCETFHCKWVFFTSKFM with signal CRRVWGKDDSSGNGNGNGSSTCIP peptide and Myc SGQPCADSDDCCETFHCKWVFFTS tag and GPI KFMCRRVWGKDGEQKLISEEDLGA anchor LCNGAGFATPVTLALVPALLATFW SLL 806 C6-C6 with long MSALLILALVGAAVASSTCIPSGQ flexible linker PCADSDDCCETFHCKWVFFTSKFM with signal CRRVWGKDDSSGGNGNGNGNGNGN peptide and Myc GNGAAAGGNGNGNGNGNGNGNGSS tag and GPI TCIPSGQPCADSDDCCETFHCKWV anchor FFTSKFMCRRVWGKDGEQKLISEE DLGALCNGAGFATPVTLALVPALL ATFWSLL

Optionally, monomer components of a dimer or multimer agent may be or become covalently linked to one another. In some embodiments, such components may be or become covalently linked to one another via one or more disulfide bonds; in some embodiments, such components may be or become covalently linked to one another via one or more peptide bonds; in some embodiments, such components may be or become covalently linked to one another via a bond other than a peptide bond. In some embodiments, such components may be or become covalently linked to one another via a linker (e.g., via a polypeptide linker). Those skilled in the art will appreciate that a linker may be comprised of any of a variety of chemical entities. In those embodiments in which a linker comprises one or a plurality of amino acids, it may be of any desired length. In some embodiments, a linker has a size (e.g., a length) that is smaller than that of one or more of the monomer components.

In some embodiments, a polypeptide component of an Hv1 modulating agent may be connected directly or via a linker sequence to a signal peptide and/or a coat protein of a phage (for phage display methods) and/or to any other domain that may alter one or more of Hv1 modulating agent expression, binding, or function.

In some embodiments, an Hv1 modulating agent may have structural modification(s). For example, an Hv1 modulating agent may be or comprise a cyclic structure, and/or may comprise a cyclic portion. For example, a polypeptide component of an Hv1 modulating agent may be cyclized such that its N-terminus is not part of the cyclic structure. In some embodiments, an Hv1 modulating agent is not cyclic and/or does not comprise any cyclic portion. In some embodiments, an Hv1 modulating agent is linear (e.g., one or more, or all, polypeptide components of an Hv1 modulating agent is/are linear polypeptide(s)). In some embodiments, an Hv1 modulating agent may be or comprise a stapled polypeptide.

In some embodiments, a polypeptide component of an Hv1 modulating agent is incorporated into a framework or scaffold structure. For example, such a polypeptide component can be incorporated into an antibody framework. Alternatively or additionally, a polypeptide component may be incorporated into a beta-sheet framework. In some embodiments, an Hv1 modulating agent may be or comprise an antibody agent or fragment or component thereof (e.g., an antigen-binding fragment or component, such as a polypeptide including sufficient CDR sequences to bind antigen comparably to an antibody). In some embodiments, an Hv1 modulating agent may be or comprise a polypeptide component that includes one or more of an immunoglobulin domain or fragment thereof. In some embodiments, an Hv1 modulating agent may be or comprise a polypeptide component that includes a domain of an immunoglobulin heavy chain. Strategies for preparing such antibody fusions are known in the art (U.S. Ser. No. 14/152,441).

Alternatively or additionally, in some embodiments, an Hv1 modulating agent may be or comprise a nucleic acid, for example that may encode a polypeptide having Hv1 modulating agent activity and/or structure, as described herein. Exemplary nucleic acid sequences for Hv1 modulating agents are illustrated in Table 2C.

Production of Hv1 Modulating Agents

Hv1 modulating agents can be produced by many methods. In some embodiments, an Hv1 modulating agent is produced by recombinant expression in a cell. In some embodiments, an Hv1 modulating agent is produced by peptide synthesis. In some embodiments, an Hv1 modulating agent is produced by in vitro translation.

Exemplary methods of designing and producing Hv1 modulating agents are presented in Example 1.

In some embodiments, an Hv1 modulating agent is presented on a replicable genetic package, e.g., in the form of a phage, yeast, ribosome, or nucleic acid-protein fusion.

In some embodiments, an Hv1 modulating agent is provided and/or utilized in the context of an expression or display system.

In some embodiments, Hv1 modulating agents are first synthesized as nucleic acids that encode polypeptide elements (e.g. elements A, B, and C in Table 3) and then annealed to produce nucleic acid sequences encoding polypeptide components (e.g. as in Table 2).

In some embodiments, a nucleic acid sequence encoding an Hv1 modulating agent may be inserted into a phagemid or phage vector, in-frame, to form a leader-linker-Hv1 modulating agent-linker-coat protein construct (Clackson and Lowman, Phage display. Oxford University Press, 2004; Barbas et al., Phage display. A laboratory manual. Cold Spring Harbor Laboratory Press, 2001). Exemplary upstream leader and downstream amino acid sequences are MAAE and GSASSA, respectively. An exemplary phage vector is pAS62. An exemplary coat protein is protein III or its truncated version. Phages can be grown, prepared, titered and stored (Clackson and Lowman, Phage display. Oxford University Press, 2004; Barbas et al., Phage display. A laboratory manual. Cold Spring Harbor Laboratory Press, 2001).

In some embodiments, Hv1 modulating agents can be inserted into vectors for expression and/or library selection. In some embodiments, a library is presented in a polypeptide array. In some embodiments, a library is presented on a replicable genetic package, e.g., in the form of a phage display, yeast display, ribosome, or nucleic acid-protein fusion library. See, e.g., U.S. Pat. No. 5,223,409; Garrard et al. (1991) Bio/Technology 9:1373-1377; WO 03/029456; and U.S. Pat. No. 6,207,446. Binding members of such libraries can be obtained by selection and screened in a high throughput format. See, e.g., U.S. 2003-0129659.

Hv1 modulating agent libraries for phage display can be generated by standard methods (Clackson and Lowman, Phage display. Oxford University Press, 2004; Barbas et al., Phage display. A laboratory manual. Cold Spring Harbor Laboratory Press, 2001). For example, Hv1 modulating agent libraries for phage display with a combinatorial arrangement of sequence elements are generated by designing overlapping or non-overlapping oligonucleotides corresponding to each individual element. These oligonucleotides are phosphorylated, annealed, mixed in a desired combination and concentration and ligated into a phagemid vector with or without linker sequences to create a library by standard methods (Sambrook et al., Molecular Cloning: A Laboratory Manual. Vols 1-3. Cold Spring Harbor Laboratory Press, 1989). Combinatorial arrangement of sequence elements to yield phage particles expressing a library of Hv1 modulating agents is demonstrated in Example 1A.

Identification and/or Characterization of Hv1 Modulating Agents

Identification and/or characterization of Hv1 modulating agents can include determining effects of candidate agents on Hv1, including Hv1 that is naturally or recombinantly expressed. In some embodiments, Hv1 is expressed in cells. In some embodiments, Hv1 is immobilized (e.g., immobilized on a solid support, an artificial membrane, or a plasma membrane of a cell). In some embodiments, Hv1 is purified.

Identification and/or characterization of Hv1 modulating agents can include the use of libraries of candidate agents.

In some embodiments, an Hv1 modulating agent is identified from a candidate library incorporated into a phage display system. In phage display, candidate Hv1 modulating agents are functionally displayed on the surface of phage and nucleic acid sequences encoding candidate Hv1 modulating agents are enclosed inside phage particles. Functional display permits selection of Hv1 modulating agents that interact with a target or targets (e.g. Hv1 channels). Selection of Hv1 modulating agents from the library can be based on the Hv1 modulating agent type (e.g., toxin type) and/or target biochemistry, pharmacology, immunology and/or other physicochemical or biological property.

A phage library can be transfected into Escherichia coli (E. coli) or other suitable bacterial species, propagated, and the phages purified. At this stage, Hv1 modulating agents or candidate agents can be functionally expressed on the surface of the phage and physically linked to their respective genes inside of the phage particle. A library is brought into contact with a target, such as Hv1 channels. For example, a phage library can be brought into contact with Hv1 channels that are immobilized on magnetic beads, as described in Example 2. After incubation with the target, those phages that express candidate Hv1 modulating agents with no or weak recognition for the target are washed away. The remaining Hv1 modulating agents that interact with the target are dissociated and can be (i) genotyped to establish the Hv1 modulating agent identity, or (ii) processed for one or more rounds of panning, or (iii) otherwise quantified and/or identified (e.g., ELISA, microbiological titering, functional testing).

Panning may be performed by the binding of candidate modulating agents to Hv1, followed by washes and modulating agent recovery. Panning may be repeated until the desired enrichment is achieved. In addition, libraries can be pre-depleted on surfaces or cells that contain no Hv1 or on an Hv1 where the putative modulating agent binding domain may be directly or indirectly altered. Additionally, any and all conditions of panning may be varied, altered or changed to achieve optimal results, such as the isolation of a specific Hv1 modulating agent. Panning variations include, but are not limited to, the presence of competing polypeptide(s), presence of excess target(s), length and temperature of binding, pre-absorption of the library on one or more different receptor(s) or cells or surfaces, composition of binding solution (e.g., ionic strength), stringency of washing, and recovery procedures. Phages recovered from panning may be processed for further rounds of panning, functional analysis, and/or sequencing/genotyping to deduce the resulting Hv1 modulating agent's amino acid sequence or biological properties (Clackson and Lowman, Phage display. Oxford University Press, 2004; Barbas et al., Phage display. A laboratory manual. Cold Spring Harbor Laboratory Press, 2001).

Following recovery after panning, Hv1 modulating agents of interest may be produced in native form by standard methods of peptide/protein synthesis/production (Sambrook et al., Molecular Cloning: A Laboratory Manual. Vols 1-3. Cold Spring Harbor Laboratory Press, 1989; Albericio, Solid-Phase Synthesis: A Practical Guide. CRC, 2000; Howl, Peptide Synthesis and Applications. Humana Press, 2005).

In some embodiments, Hv1 modulating agents are tested for activity toward recombinant or functional Hv1. Samples that include functional channels (e.g., cells or artificial membranes) can be treated with an Hv1 modulating agent and compared to control samples (e.g., samples without the Hv1 modulating agent), to examine the extent of modulation. In some embodiments, Hv1 may be naturally expressed.

In some embodiments, cells may be stably or transiently transfected with functional Hv1. For example, HEK-293T (mammalian human embryonic kidney) cells may be transfected with Hv1 (e.g. human Hv1 or human Hv1 tagged with a fluorescent protein) for transient expression. In one example, HEK-293T cells transiently expressing hHv1 tagged with teal fluorescent protein are used in patch clamp electrophysiology to determine effects of the Hv1 modulating agents C5 or C6 on proton currents.

Changes in proton flux may be assessed by determining changes in polarization (i.e., electrical potential) of a cell or membrane expressing Hv1. In some embodiments, a change in cellular polarization is measured by measuring changes in current (thereby measuring changes in polarization) with voltage-clamp and patch-clamp techniques, e.g., the “cell-attached” mode, the “inside-out” mode, and the “whole cell” mode (see, e.g., Ackerman et al., New Engl. J. Med. 336:1575-1595, 1997). Whole cell currents can be determined using standard methodology (see, e.g., Hamil et al., PFlugers. Archiv. 391:85, 1981). Other assays include radiolabeled rubidium flux assays and fluorescence assays using voltage sensitive dyes (see, e.g., Vestergarrd-Bogind et al., J. Membrane Biol. 88:67-75, 1988; Daniel et al., J. Pharmacol. Meth. 25:185-193, 1991; Holevinsky et al., J. Membrane Biology 137:59-70, 1994). In some embodiments, candidate Hv1 modulating agents are present in the range from 1 pM to 100 mM. Other methods for assessing Hv1 modulating agent effects on proton flux are described in the Examples herein.

Hv1 modulating agents can also be identified or characterized by evaluating processes at the cellular, tissue and/or organism level. For example, Hv1 modulating agents can be evaluated for effects downstream of Hv1 activity or signaling. Various effects of Hv1 modulating agents that may be determined using intact cells or animals include transcriptional changes, changes in cell metabolism, and changes in intracellular second messengers.

In some embodiments, Hv1 modulating agents can be evaluated for effects on human sperm. For example, Hv1 modulating agents can be evaluated for effects on sperm capacitation-related processes, including changes in sperm motility, decrease of cholesterol in the membranes, increase of tyrosine phosphorylation in several proteins, or maturation of the sperm response to progesterone. Capacitation of spermatozoa occurs along with an increase in the amplitude of voltage-gated proton current. Known Hv1 inhibitor, Zn²⁺, reduces H⁺ current in sperm cells. Accordingly, an Hv1 modulating agent can be evaluated for suppression of such sperm capacitation-related processes. Alternatively, an Hv1 modulating agent can be evaluated for enhancing sperm capacitation-related processes. Alternatively or additionally, an Hv1 modulating agent can be evaluated for non-capacitation-related processes that affect sperm activation, mobility, and/or fertilization.

In some embodiments, Hv1 modulating agents can be evaluated for effects on cells that function in the immune system. For example, Hv1 is expressed in white blood cells (WBCs). Hv1 in WBCs has been shown to compensate charge buildup on the cell membrane during production of ROS. Hv1 knockout or inhibition impairs ROS production in these cells. Accordingly, an Hv1 modulating agent can be evaluated for suppression of ROS production in WBCs.

Hv1 modulating agents can be selected for their potency and selectivity of modulation of Hv1. For example, an Hv1 modulating agent that demonstrates low IC₅₀ value for Hv1, and a higher IC₅₀ value for other ion channels within the test panel, is considered to be selective toward Hv1.

Compositions

The present disclosure also features compositions that include and/or deliver Hv1 modulating agents.

In some embodiments, a composition is a pharmaceutically acceptable composition that includes and/or delivers an Hv1 modulating agent described herein. For example, in some embodiments, a provided composition includes an Hv1 modulating agent polypeptide component. Alternatively or additionally, in some embodiments, a provided composition includes a nucleic acid that encodes an Hv1 modulating agent polypeptide component, a cell that expresses (or is adapted to express) an Hv1 modulating agent polypeptide component, etc. In some embodiments Hv1 modulating agents having any of the modifications of the present disclosure are included in pharmaceutical compositions.

General considerations in the formulation and manufacture of pharmaceutical agents may be found, for example, in Remington's Pharmaceutical Sciences, 19^(th) ed., Mack Publishing Co., Easton, Pa., 1995.

Pharmaceutical compositions may be in a variety of forms. These include, for example, liquid, semi-solid and solid dosage forms, such as liquid solutions (e.g., injectable and infusible solutions), dispersions or suspensions, microemulsions, liposomes and suppositories. The proper fluidity of a solution can be maintained, for example, by the use of a coating such as lecithin, by the maintenance of the required particle size in the case of dispersion and by the use of surfactants. Prolonged absorption of injectable compositions can be brought about by including in the composition an agent that delays absorption, for example, monostearate salts and gelatin. The preferred form of pharmaceutical composition depends on the intended mode of administration and therapeutic application. Typical compositions are in the form of injectable or infusible solutions, such as compositions similar to those used for administration of antibodies to humans.

The pharmaceutical composition can include a pharmaceutically acceptable carrier. For example, pharmaceutical compositions can include a therapeutic agent in addition to one or more inactive agents such as a sterile, biocompatible carrier.

Exemplary carriers include any and all solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents, and the like that are physiologically compatible. For example, carriers may include sterile water, saline, buffered saline, or dextrose solution. Alternatively or additionally, the composition can contain any of a variety of additives, such as stabilizers, buffers, excipients (e.g., sugars, amino acids, etc.), or preservatives. Preferably, the carrier is suitable for oral, intravenous, intramuscular, subcutaneous, parenteral, spinal or epidermal administration (e.g., by injection or infusion).

The pharmaceutical composition can include a pharmaceutically acceptable salt, e.g., a salt that retains the desired biological activity of the Hv1 modulating agent and does not impart any undesired toxicological effects (see e.g., Berge, S. M., et al., J. Pharm. Sci. 66:1-19, 1977).

Depending on the route of administration, the Hv1 modulating agent may be coated in a material to protect the compound from the action of acids and other natural conditions that may inactivate the compound.

In certain embodiments, a pharmaceutical composition can include a therapeutic agent that is encapsulated, trapped, or bound within a lipid vesicle, a bioavailable and/or biocompatible and/or biodegradable matrix, or other microparticles.

In certain embodiments, an Hv1 modulating agent is prepared with a carrier that protects against rapid release, such as a controlled release formulation, including implants, and microencapsulated delivery systems. Biodegradable, biocompatible polymers can be used, such as ethylene vinyl acetate, polyanhydrides, polyglycolic acid, collagen, polyorthoesters, and poly lactic acid. Many methods for the preparation of such formulations are patented or generally known. See, e.g., Sustained and Controlled Release Drug Delivery Systems, J. R. Robinson, ed., Marcel Dekker, Inc., New York, 1978. Pharmaceutical formulation is a well-established art, and is further described in Gennaro (ed.), Remington: The Science and Practice of Pharmacy, 20.sup.th ed., Lippincott, Williams & Wilkins, 2000 (ISBN: 0683306472); Ansel et al., Pharmaceutical Dosage Forms and Drug Delivery Systems, 7.sup.th Ed., Lippincott Williams & Wilkins Publishers, 1999 (ISBN: 0683305727); and Kibbe (ed.), Handbook of Pharmaceutical Excipients American Pharmaceutical Association, 3rd ed., 2000 (ISBN: 091733096X).

In some embodiments, a provided pharmaceutical composition will include an Hv1 modulating agent that is not aggregated. For example, in some embodiments, less than 1%, 2%, 5%, 10%, 20%, or 30%, by dry weight or number, of Hv1 modulating agent is present in an aggregate.

In some embodiments, a provided pharmaceutical composition will include an Hv1 modulating agent that is not denatured. For example, less than 1%, 2%, 5%, 10%, 20%, or 30%, by dry weight or number, of Hv1 modulating agents administered is denatured.

In some embodiments, a provided pharmaceutical composition will include an Hv1 modulating agent that is not inactive. For example, less than 1%, 2%, 5%, 10%, 20%, or 30%, by dry weight or number, of Hv1 modulating agents administered is inactive.

In some embodiments, pharmaceutical compositions are formulated to reduce immunogenicity of provided Hv1 modulating agents. For example, in some embodiments, a provided Hv1 modulating agent is associated with (e.g., bound to) an agent, such as polyethylene glycol and/or carboxymethyl cellulose, that masks its immunogenicity. In some embodiments, a provided binding agent has additional glycosylating that reduces immunogenicity.

Kits

Also provided by the present disclosure are kits that include an Hv1 modulating agent described herein and instructions for use, e.g., treatment, prophylactic, or diagnostic use.

In addition to the Hv1 modulating agent, the composition of the kit can include other ingredients, such as a solvent or buffer, a stabilizer or a preservative, and/or a second agent for treating a condition or disorder described herein. Alternatively, other ingredients can be included in the kit, but in different compositions or containers than the Hv1 modulating agent. In such embodiments, the kit can include instructions for admixing the Hv1 modulating agent and the other ingredients, or for using the Hv1 modulating agent together with the other ingredients.

Alternatively or additionally, contents of kits may include, but are not limited to, expression plasmids containing nucleotides (or characteristic or biologically active portions) encoding Hv1 modulating agents of interest (or characteristic or biologically active portions). Alternatively or additionally, kits may contain expression plasmids that express Hv1 modulating agents of interest (or characteristic or biologically active portions). Alternatively or additionally, kits may contain isolated and stored Hv1 modulating agents.

In certain embodiments, kits for use in accordance with the present invention may include, a reference sample, instructions for processing samples, performing tests on samples, instructions for interpreting the results, buffers and/or other reagents necessary for performing tests. In certain embodiments the kit can comprise a panel of antibodies.

The present invention provides kits for administration of pharmaceutical compositions. For example, in some embodiments, the invention provides a kit comprising at least one dose of an Hv1 modulating agent. In some embodiments, the invention provides a kit comprising an initial unit dose and one or more subsequent unit doses of an Hv1 modulating agent. In some such embodiments, the initial unit dose is greater than the subsequent unit doses or wherein the all of the doses are equal.

Methods of Administration

Pharmaceutical compositions may be administered in any dose appropriate to achieve a desired outcome. In some embodiments, the desired outcome is reduction in intensity, severity, and/or frequency, and/or delay of onset of one or more symptoms of an Hv1 associated disease or condition.

A therapeutically effective amount of an Hv1 modulating agent composition can be administered, typically an amount which is effective, upon single or multiple dose administration to a subject, in treating a subject, e.g., curing, alleviating, relieving or improving at least one symptom of a disease or condition in a subject to a degree beyond that expected in the absence of such treatment. A therapeutically effective amount of the composition may vary according to factors such as the disease state, age, sex, and weight of the individual, and the ability of the compound to elicit a desired response in the individual. A therapeutically effective amount is also one in which any toxic or detrimental effects of the composition is outweighed by the therapeutically beneficial effects. A therapeutically effective dosage preferably modulates a measurable parameter, favorably, relative to untreated subjects. The ability of an Hv1 modulating agent to inhibit a measurable parameter can be evaluated in an animal model system predictive of efficacy in a human disorder.

In some embodiments, pharmaceutical compositions are administered in multiple doses. In some embodiments, pharmaceutical compositions are administered in multiple doses/day. In some embodiments, pharmaceutical compositions are administered according to a continuous dosing regimen, such that the subject does not undergo periods of less than therapeutic dosing interposed between periods of therapeutic dosing. In some embodiments, pharmaceutical compositions are administered according to an intermittent dosing regimen, such that the subject undergoes at least one period of less than therapeutic dosing interposed between two periods of therapeutic dosing.

Dosage regimens can be adjusted to provide the optimum desired response (e.g., a therapeutic response). For example, a single bolus may be administered, several divided doses may be administered over time or the dose may be proportionally reduced or increased as indicated by the exigencies of the therapeutic situation. It is especially advantageous to formulate parenteral compositions in dosage unit form for ease of administration and uniformity of dosage. Dosage unit form as used herein refers to physically discrete units suited as unitary dosages for the subjects to be treated; each unit contains a predetermined quantity of ligand calculated to produce the desired therapeutic effect in association with the required pharmaceutical carrier.

An exemplary, non-limiting range for a therapeutically or prophylactically effective amount of an Hv1 modulating agent described herein is 0.1-20 mg/Kg, more preferably 1-10 mg/Kg. In some embodiments, an agent can be administered by parenteral (e.g., intravenous or subcutaneous) infusion at a rate of less than 20, 10, 5, or 1 mg/min to reach a dose of about 1 to 50 mg/m² or about 5 to 20 mg/m². It is to be noted that dosage values may vary with the type and severity of the condition to be alleviated. It is to be further understood that for any particular subject, specific dosage regimens should be adjusted over time according to the individual need and the professional judgment of the person administering or supervising the administration of the compositions (e.g., the supervising physician), and that dosage ranges set forth herein are only exemplary.

Pharmaceutical compositions of the present invention can be administered by a variety of routes, including oral, intravenous, intramuscular, intra-arterial, subcutaneous, intraventricular, transdermal, interdermal, rectal, intravaginal, intraperitoneal, topical (as by powders, ointments, creams, or drops), mucosal, nasal, buccal, enteral, sublingual; by intratracheal instillation, bronchial instillation, and/or inhalation; and/or as an oral spray, nasal spray, and/or aerosol. For example, for therapeutic applications, an Hv1 modulating agent composition can be administered by intravenous infusion at a rate of less than 30, 20, 10, 5, or 1 mg/min to reach a dose of about 1 to 100 mg/m² or 7 to 25 mg/m². Alternatively, the dose could be 100 μg/Kg, 500 μg/Kg, 1 mg/Kg, 5 mg/Kg, 10 mg/Kg, or 50 mg/Kg. The route and/or mode of administration will vary depending upon the desired results. In general the most appropriate route of administration will depend upon a variety of factors including the nature of the agent (e.g., its stability in the environment of the gastrointestinal tract), the condition of the patient (e.g., whether the patient is able to tolerate oral administration), etc.

A common mode of administration is parenteral (e.g., intravenous, intramuscular, intraarterial, intrathecal, intracapsular, intraorbital, intracardiac, intradermal, intraperitoneal, transtracheal, subcutaneous, subcuticular, intraarticular, subcapsular, subarachnoid, intraspinal, epidural and intrasternal injection and infusion). In one embodiment, the Hv1 modulating agent composition is administered by intravenous infusion or injection. In another embodiment, the Hv1 modulating agent composition is administered by intramuscular or subcutaneous injection. In another embodiment, the Hv1 modulating agent composition is administered orally. In some embodiments, the Hv1 modulating agent composition is administered topically. In some embodiments, the Hv1 modulating agent composition is administered transdermally. Pharmaceutical compositions typically must be sterile and stable under the conditions of manufacture and storage.

Hv1 modulating agents or pharmaceutical compositions of the present disclosure may be administered either alone or in combination with one or more other agents. In some embodiments, Hv1 modulating agents or pharmaceutical compositions of the present disclosure may be administered with one or more other Hv1 modulating agents. In some embodiments, Hv1 modulating agents or pharmaceutical compositions of the present disclosure may be administered with one or more other pharmaceutical agent including, but not limited to, small molecules, vaccines and/or antibodies. In some embodiments, Hv1 modulating agents or pharmaceutical compositions may be administered in combination with an adjuvant.

Combinations of agents may be administered at the same time or formulated for delivery together. Alternatively, each agent may be administered at a dose and on a time schedule determined for that agent. Additionally, the invention encompasses the delivery of the pharmaceutical compositions in combination with agents that may improve their bioavailability, reduce or modify their metabolism, inhibit their excretion, or modify their distribution within the body. Although the pharmaceutical compositions of the present invention can be used for treatment of any subject (e.g., any animal) in need thereof, they are most preferably used in the treatment of humans.

Uses

As described herein, Hv1 channels have been reported to play a role in a variety of biological processes, and to impact various diseases, disorders, and conditions.

The present disclosure encompasses treatment of Hv1 associated diseases or conditions. Hv1 modulating agents and/or Hv1 modulating agent compositions described herein can be administered, alone or in combination with, another agent to a subject, e.g., a patient, e.g., a patient who has a disorder (e.g., an Hv1-associated disease or condition, e.g. immune deficiency), a symptom of a disorder or a predisposition toward a disorder, with the purpose to cure, heal, alleviate, relieve, alter, remedy, ameliorate, improve or affect the disorder, the symptoms of the disorder or the predisposition toward the disorder. The treatment may also delay onset, e.g., prevent onset, or prevent deterioration of a condition.

In some embodiments, Hv1 modulating agent pharmaceutical compositions are administered to a subject suffering from or susceptible to an Hv1 associated disease or condition. In some embodiments, a subject is considered to be suffering from an Hv1 associated disease or condition if the subject is displaying one or more symptoms commonly associated with said disease or condition. Hv1 modulating agents or Hv1 modulating agent compositions may be administered prior to or after development of one or more such symptoms.

For example Hv1 modulating agents may be used to ameliorate inflammation, allergies, autoimmunity, cancer, asthma, brain damage from ischemic stroke, Alzheimer's disease, infertility, and numerous other conditions. In some embodiments, the desired outcome is reduction in intensity, severity, and/or frequency, and/or delay of onset of one or more of these conditions. Additionally or alternatively, Hv1 modulating agents may be used as a form of birth control by blocking sperm function.

Additionally, Hv1 modulating agents may be used to change any of the functions of Hv1 channels described in the present disclosure to achieve a preferred or therapeutic outcome. As described herein, Hv1 channels transport protons across cell membranes and are expressed in a variety of cells and tissues. Functions of Hv1 channels differ depending on the cells in which they are expressed. Uses for Hv1 modulating agents can include increasing or decreasing proton current across cell membranes and/or increasing or decreasing pH in the cytosolic, extracellular, or intraluminal space of cells.

In some embodiments, uses for Hv1 modulating agents may include effects on Hv1-related processes. For example, in some embodiments, Hv1 modulating agents may be used to increase or decrease the expression and/or function of NOX enzymes, including NOX1, NOX2, NOX3, and/or NOX4. In some embodiments, Hv1 modulating agents may be used to increase or decrease production of ROS.

In some embodiments, uses for Hv1 modulating agents may include altering biological functions in specific cells. For example, the function of Hv1 channels in white blood cells includes extrusion of protons to facilitate ROS production via NOX activity in the phagosome. This process allows white blood cells to destroy bacteria and other pathogens. In some embodiments, uses of Hv1 modulating agents may include changing these functions in white blood cells. Alternatively, Hv1 channel function in human sperm has been associated with sperm capacitation, activation and mobility to achieve fertilization. In some embodiments, Hv1 modulating agent uses may include increasing or decreasing sperm function and/or fertilization ability.

While various aspects and examples have been described, it will be apparent to those of ordinary skill in the art that many more examples and implementations are possible within the scope of this disclosure. Accordingly, the disclosure is not to be restricted except in light of the attached claims and their equivalents.

EXEMPLIFICATION Example 1: Designing Hv1 Modulating Agents

The present Example describes certain Hv1 modulating agents provided herein. Certain Hv1 modulating agents provided herein comprise a polypeptide component having an amino acid sequence including element(s) found in wild-type toxin polypeptides. In some embodiments, exemplary Hv1 modulating agents comprise a polypeptide component whose amino acid sequence further comprises one or more tag elements (e.g., a detectable tag, a localizing tag, etc). In some embodiments, exemplary Hv1 modulating agents have a structure that comprises both a polypeptide component and a non-polypeptide component (e.g., a modifying component such as a lipid-containing moiety, a saccharide-containing moiety, etc). Alternatively or additionally, in some embodiments, exemplary Hv1 modulating agents are multimeric in that their structure includes multiple (e.g., 2 or more) monomer components associated with one another. In some embodiments, all monomers in a multimer are structurally identical (or substantially identical) to one another. In some embodiments, a multimer may comprise 2 or more distinct monomers. In some embodiments, two or more monomers in a multimer may be covalently associated with one another (e.g., via a linker or cross-linker).

A. Toxin Sequences

As noted above, certain Hv1 modulating agents provided herein have an amino acid sequence including element(s) found in wild-type toxin polypeptides. Representative such agents were designed as described below.

The amino acid sequence of the Peruvian green velvet tarantula (Thrixopelma pruriens) was used as a template to identify predicted wild-type toxin sequences using the basic local alignment search tool (BLAST) in the UniProt and Pfam databases. A total of 110 predicted wild-type toxin sequences were identified (Table 1). All of these sequences encode a polypeptide characterized as having an inhibitor cysteine knot (ICK) structural motif. The amino acid sequences of these 110 predicted wild-type toxins were aligned around six conserved cysteine residues of the ICK motif. Three sequence elements, A, B, and C were delineated by the second and fifth of the six conserved cysteine residues in each predicted wild-type toxin sequence, resulting in 95 A, 104 B, and 106 C sequence elements (Table 3). Nucleotides were synthesized corresponding to these A, B, and C elements.

Complementary nucleotide pairs for each unique element A, B, or C, were synthesized to produce nucleotide duplexes. These nucleotide duplexes were phosphorylated using T4 Polynucleotide Kinase and annealed unidirectionally to produce polynucleotide components having an A-B-C sequence element pattern linked at cysteine residues. To achieve and monitor incorporation of the sequence elements, 104 separate reactions were performed to ligate the ABC inserts into the pAS62 phagemid vector in frame with phage particle coat protein pIII, resulting in phagemids having the ABC inserts (see, e.g., PCT/US2008/013385). Each reaction contained one B nucleotide duplex, 95 A nucleotide duplexes, and 106 C nucleotide duplexes. Ligation mixtures were transformed in SS320 electrocompetent cells (Lucigen, Middleton, Wis.). To verify unbiased insert utilization, 416 plaques were sequenced. The processes yielded phage particles expressing the original 110 predicted wild-type toxins and approximately 1,047,170 novel peptides. Exemplary novel peptides are listed in Table 2A and FIG. 1. Exemplary A, B and C sequence elements are listed in Table 3.

B. Linkers and Dimerization

Certain exemplary Hv1 modulating agents were prepared by linking together two polypeptide components, each of which had an amino acid sequence comprising elements of wild-type toxin polypeptides as described above in Section A.

For example, two monomers of the agent labeled as “C6” in Table 2A were joined together via a peptide linker. Several different peptide linkers were utilized. For example, each of a rigid linker of 10 amino acid residues, a flexible linker of 10 amino acid residues, or a long flexible linker of 38 amino acid residues was used. Table 4A lists amino acid sequences of exemplary polypeptides created through such linkage.

C. Signal Peptides

In some embodiments, one or more signal peptides can be included in exemplary Hv1 modulating agents (Table 4B).

For example, Hv1 modulating agents with an N-terminal trypsin secretory signal sequence can be prepared.

D. Detectable Tags

In some embodiments, an Hv1 modulating agent may be modified with an epitope tag.

For example, a c-Myc epitope tag can be added near the C-terminus of a polypeptide component in an Hv1 modulating agent (Table 4C).

E. Tethering Moieties

In some embodiments, an Hv1 modulating agent may be modified with a tethering moiety that targets the Hv1 modulating agent to a specific surface.

For example, a hydrophobic sequence may be added to the C-terminus of an Hv1 modulating agent that targets the Hv1 modulating agent for covalent tethering to glycosylphosphatidylinositol (GPI) anchors inserted in the extracellular leaflet of the plasma membrane (Table 4D).

Annotated sequences of exemplary modified Hv1 modulating agents are presented in FIG. 3.

F. Generating Hv1 Modulating Agents with Linkers and Modifications

Representative Hv1 modulating agents having signal peptides, detectable tags, and tethering moieties were generated as follows. The sequence encoding mammalian Lynx1, a toxin-like nicotinic acetylcholine receptor modulator, was replaced by cDNA of the Hv1 modulating agent C6, in-frame between the secretion signal and the Lynx1 hydrophobic sequence for GPI attachment. A flexible linker containing a glycine-asparagine repeat was inserted between the C6 sequence and the hydrophobic sequence for GPI attachment, and a c-Myc epitope tag was introduced in the middle of the linker. Hv1 modulating agents having these modifications are also called “T-toxins.” Exemplary T-toxin sequences are depicted in FIGS. 3A-3E. The present disclosure appreciates that methods analogous to those described in Gui, J. et al., “A tarantula-venom peptide antagonizes the TRPA1 nociceptor ion channel by binding to the S1-S4 gating domain,” Curr Biol. 24(5):473-83 (2014) can be employed to generate GPI-tethered toxins as described herein.

Example 2: Characterization of Hv1 Modulating Agents

The present Example demonstrates a high-throughput assay for characterization of Hv1 modulating agents. Specifically, this assay characterizes whether Hv1 modulating agents are capable of binding human Hv1 (hHv1) protein.

To characterize if an Hv1 modulating agent can bind to hHv1 channels, a phage display library expressing Hv1 modulating agents was generated. Phage particles from Example 1A were used to infect Escherichia coli (E. coli) XL1-Blue cells for 15 min at room temperature. The infected cells were grown overnight at 37° C. in 150 mL 2×YT in the presence of 1010/mL M13K07 helper phage, 100 g/mL ampicillin, and 0.1 mM isopropyl (3-D-1-thiogalactopyranoside (IPTG). Cultures were centrifuged and the supernatant was precipitated with PEG/NaCl solution. The phage pellet was collected by centrifugation and dissolved in TBS. Phage particle titer was determined by serial dilution in TBS and infection of E. coli XL1-Blue followed by plating on LB plates with antibiotic and determination of colony forming units (cfu).

hHv1 protein was biotinylated using sulfosuccinimidyl 2-(biotinamido)-ethyl-1,3-dithiopropionate (EZ-Link Sulfo-NHS-SS-Biotin, Thermo Scientific). Biotinylation was verified by a pull-down assay using streptavidin MagneSphere beads (Promega). Biotinylated hHv1 was adsorbed to 300 μl streptavidin MagneSphere paramagnetic particles, and free streptavidin-binding sites were blocked with biotin to prevent nonspecific binding.

After manual washing of the magnetic beads, library phage particles (10¹¹ cfu) were added in 300 μL TBSB (25 mM Tris-HCl, 140 mM NaCl, 3 mM KCl, 2 mM LPPG, 0.5% bovine serum albumin, pH 7.4) and incubated on a rocking shaker for 1 h. Poorly adherent phage particles were removed by washing 2-5 times with TBSTB (TBSB with 0.1% Tween 20). The captured phages on the magnetic beads were eluted with 100 mM DTT in 20 mM Tris, pH 8.0, for 10 min, and then used to infect E. coli XL1-Blue cells (Stratagene) for phage amplification. The phage particles captured in the first round were cycled through an additional five rounds of binding and selection using an automated magnetic bead manipulator (KingFisher, Thermo Scientific). Phage particles were quantified by titering before and after selective library sorting and genotyped by DNA sequencing after six rounds of panning. Phage enrichment was observed with immobilized hHv1 as the target compared with the control target streptavidin. Exemplary Hv1 modulating agents enriched by this method are listed in Table 2A. In some instances, repeats of Hv1 modulating agent sequences after several rounds of panning can be observed, as demonstrated by agents labeled as A6 and G2, C2 and F2, C6 and D5, and D6 and E2. Without wishing to be bound by any particular theory, any repeat may be considered significant (since the library had more than 1 million peptides initially) and may demonstrate selection and functional convergence.

Example 3: Characterization of Hv1 Modulating Agents by T-Toxin Assay

The present example demonstrates characterization of the effects of Hv1 modulating agents on hHv1 using T-toxins. Specifically, the present example demonstrates inhibition of hHv1 function as measured by tail current from Xenopus laevis oocytes expressing only hHv1 or both hHv1 and Hv1 modulating agents tethered to the oocyte plasma membrane.

T-toxin cDNAs were cloned into the pCS2+ plasmid vector for in vitro transcription of T-toxin cRNA. Capped cRNAs were prepared by restriction enzyme linearization, followed by in vitro transcription reaction with SP6 (for T-toxins) and T7 (for hHv1) RNA polymerase (mMessenger mMachine kit, Ambion). Concentrations of cRNAs were measured using NanoDrop 2000 (Thermo Scientific).

cRNAs for T-toxins and hHv1 were mixed at 1:1 ratio (w/w) and injected into the Xenopus laevis oocytes. Currents were measured by Two Electrode Voltage Clamp (TEVC). Recording solution was (in mM): 90 NaCl, 1 MgCl₂, 2 CaCl₂), 120 HEPES, pH 7.3. Recordings were performed with constant gravity flow of solution at 2 ml/min yielding chamber exchange in ˜5 s. Currents were recorded 2-3 days after cRNA injection using an oocyte clamp amplifier OC-725C (Warner Instruments, Hamden, Conn.), and electrodes filled with 3 M KCl with resistance of 0.3-1 MΩ. Data were filtered at 1 kHz and digitized at 20 kHz using pClamp software and assessed with Clampfit v9.0 and Origin 6.0. Inhibition was studied by comparing tail current from oocytes expressing only hHv1 and those with both hHv1 and T-toxins. Inhibition was calculated as unblocked fractional current (FIG. 3F).

Example 4: Characterization of Hv1 Modulating Agents with a Transmembrane Link

The present example demonstrates characterization of Hv1 modulating agent effects on hHv1 using Hv1 modulating agents expressed from cells via a transmembrane link.

The Hv1 modulating agent C6 was tethered to cell surfaces using a transmembrane domain from the PDGF receptor, which links an internal mVenus fluorescent protein to an external C6 (FIG. 7). Unlike the tether in oocytes which attaches C6 to the outside of the cell (e.g. FIG. 3), this is a transmembrane link. To transiently express hHv1, 1 μg of hHv1 tagged with teal fluorescence protein (hHv1-TFP) was transfected into HEK-293T cells using Lipofectamine 2000. Changes in the single exponential fit of fluorescence decay were indicative of FRET (FIG. 8). Changes in current density and shifts in the g_(H)-V were indicative of blocking of hHv1.

Example 5: Hv1 Modulating Agents Activate or Inhibit Hv1 Proton Current

The present Example documents assessing activity of the voltage-gated proton channel Hv1 in response to Hv1 modulating agents. Activity of Hv1 was assessed by changes in proton currents.

To transiently express hHv1, 1 μg of hHv1 or hHv1 tagged with teal fluorescence protein (hHv1-TFP) was transfected into HEK-293T cells using Lipofectamine 2000. In some instances, green fluorescent protein was used as a transfection marker. Transfected cells were plated onto glass coverslips. Green or teal cells were selected for whole-cell patch clamp after 24 hours.

Patch clamp recordings were performed with an external solution of 100 mM HEPES, pH 7.5, 70 mM NaCl, and 10 mM glucose. The pipette solution was 100 mM Bis Tris buffer, pH 6.5, 70 mM NaCl and 10 mM glucose. Hv1 modulating agent was applied to these cells while pulsing to 40 mV every 10 seconds and proton currents were measured using whole-cell patch clamp electrophysiology.

FIG. 4 shows activation or inhibition of Hv1 proton currents by Hv1 modulating agent as compared to current without addition of modulating agent. Cells were incubated with either 500 nM C5 (FIG. 4A) or 250 nM C6 (FIG. 4B). Activation of Hv1 channels by C5 increased proton current and slowed channel closing. Block of Hv1 channels by C6 decreased proton currents.

Example 6: Hv1 Modulating Agent Inhibits Effects of Progesterone on Sperm Capacitation

The present example demonstrates effectiveness of certain Hv1 modulating agents in suppressing maturation of the sperm response to progesterone. This example shows that activity of Hv1 channels during capacitation is necessary for calcium rise and acrosomal reaction stimulation by physiological inducers required for fertilization.

To test effects of Hv1 modulating agents on sperm capacitation in a blind study, human sperm was exposed to capacitating conditions in the presence or absence of Hv1 modulating agent C6 (Tx C) or a control peptide (Tx A) having the amino acid sequence GVEINVKCSGSPQCLKPCKDAGMDFGDCMNDKCHCTPK (SEQ ID NO: 810) (a mutant scorpion venom peptide; Takacs, Z., et al., “A designer ligand specific for Kv1.3 channels from a scorpion neurotoxin-based library,” Proc Natl Acad. Sci. USA. 106(52): 22211-22216 (2009)). Sperm were incubated for 1 hour with the Tx C or Tx A (20 μM) in a medium that does not promote capacitation. Cells were transferred to a capacitating medium with Tx C or Tx A. After 4 hours of incubation, parameters related to capacitation were analyzed (FIG. 5). Known protocols for such analyses are described in Pocognoni, C. A., et al., “Perfringolysin O as a useful tool to study human sperm physiology,” Fertility and Sterility, 99(1): p. 99-106.e2 (2013).

C6 did not affect the vitality (FIG. 5A), the protein tyrosine phosphorylation (FIG. 5F and FIG. 5G), or the cholesterol content of the membranes (FIG. 5H). C6 did not significantly alter the mobility of sperm (FIGS. 5B-5E). C6 did affect the response of sperm to progesterone. The increase of cytosolic calcium triggered by progesterone is diminished in the presence of the peptide modulator and the acrosome reaction induced by the hormone is inhibited (FIGS. 5I-5K). Moreover, when C6 was added after capacitation, both intracellular calcium and acrosomal reaction, triggered by progesterone, did not show any changes.

Example 7: Hv1 Modulating Agents Inhibit Production of Reactive Oxygen Species in Human Blood Cells

The present example demonstrates effectiveness of certain Hv1 modulating agents in blocking ROS production by human blood cells.

Whole blood was purchased in 10 mL tubes from Innovative Research, Inc, in accordance with FDA guidelines. Blood was used within 24-48 hours after being drawn. Upon arrival, blood cells were counted using a hemocytometer and diluted in Tyrode's solution to approximately 5×10⁶ cells/mL. Twenty μL of the dilute blood cells were added to each well of a 96-well plate with a total volume of 100 μL in Tyrode's solution. Reactive oxygen species (ROS) were detected by fluorescence readout using 100 μM Amplex Red with 2 units/mL horseradish peroxidase added to each well.

Blood was incubated with the following treatment conditions for 1 hour at 37 C: control; 100 μM zinc; 100 pM — 5 μM C6; and 10 μM MOKA toxin. Each treatment condition was added to wells in 5 repeats. After the incubation, 200 nM phorbol myristate acetate (PMA) was added to all wells except the control. PMA was used to stimulate ROS production. Fluorescence measurements were taken immediately after using excitation at 530 nM and emission at 590 nM. Measurements were repeated every 15 to 30 min for the next 2 hours. Relative fluorescence intensity was plotted versus time and used to calculate inhibition. FIG. 6 demonstrates that C6 blocks production of ROS in human blood cells in a dose-dependent manner. The known inhibitor of Hv1, zinc, blocks ROS production to background (control) levels. Two toxins that block potassium channels with nM affinity (Moka and KTX) had no effect.

Example 8: The Hv1 Modulating Agent C6 Targets an S3-S4 External Loop Region of hHv1

The present example demonstrates identification of regions in hHv1 that can bind and/or respond to modulation by the Hv1 modulating agent C6.

The Hv1 modulating agent C6 did not inhibit proton current of Ciona intestinalis (C. intestinalis) Hv1 channels (CiHv1). Chimeric forms of ciHv1 were generated in which amino acids from human Hv1 (hHv1) corresponding to the S3-S4 external loop replaced the same region of CiHv1 (hS3-S4-ciHv1). The resulting hS3-S4-ciHv1 chimera comprised hHv1 amino acids 1183 to L204: ILDIVLLFQEHQFEALGLLILL (SEQ ID NO: 111) and maintained characteristics of Hv1 currents. C6 blocked current for hS3-S4-ciHv1 (FIGS. 9A and 9B). A different chimeric form of ciHv1 (shortC), comprised hHv1 amino acids 1183 to F195: ILDIVLLFQEHQF (SEQ ID NO: 112). The shortC chimera had very low currents (approximately 100 pA), and was responsive to C6 inhibition (FIG. 9A).

Twelve residues in the S3-S4 external loop region of hHv1 (F190 to L201) were individually mutated to Cysteine. Current with 1 μM C6 normalized to current without toxin (Itox/Ictr) was measured (FIG. 9C). Mutating hHv1 E192C increased normalized current with C6 compared to WT hHv1. Mutating hHv1 G199C or G199L increased inhibitory effects of C6 compared to WT hHv1.

EQUIVALENTS

Those skilled in the art will recognize, or be able to ascertain using no more than routine experimentation, many equivalents to the specific embodiments of the invention described herein. The scope of the present invention is not intended to be limited to the above Description, but rather is as set forth in the following claims. 

1. A voltage-gated proton channel (Hv1) inhibitor comprising at least two engineered polypeptide components, wherein each component has an amino acid sequence: (SEQ ID NO: 129) SSTCIPSGQPCADSDDCCETFHCKVVVFFTSKFMCRRVWGKD.

2-25. (canceled)
 26. The Hv1 inhibitor of claim 1, wherein at least one of the at least two polypeptide components comprises one or more pendant groups or a modification selected from the group consisting of acetylation, amidation, glycosylation, lipidation, methylation, pegylation, phosphorylation, and combinations thereof.
 27. The Hv1 inhibitor of claim 1, wherein at least one of the at least two polypeptide components comprises one or more tag elements, wherein optionally the one or more tag elements comprises a detectable tag or a localizing tag.
 28. The Hv1 inhibitor of claim 1, wherein at least one of the at least two polypeptide components is connected to a signal peptide or a coat protein of a phage.
 29. The Hv1 inhibitor of claim 1 fabricated as a dimer comprising two engineered polypeptide components. 30-31. (canceled)
 32. The Hv1 inhibitor of claim 1, wherein the engineered polypeptide components are linked together via a peptide linker. 33-34. (canceled)
 35. A cell comprising or having contained therein an Hv1 inhibitor of claim
 1. 36. The Hv1 inhibitor of claim 1 incorporated into an antibody framework.
 37. The Hv1 inhibitor of claim 36, wherein the Hv1 inhibitor is fused to an antibody sequence or fragment thereof.
 38. The Hv1 inhibitor of claim 36, wherein the Hv1 inhibitor is attached or inserted into one or more of an immunoglobulin domain or fragment thereof. 39-79. (canceled)
 80. A pharmaceutical composition comprising: of an Hv1 inhibitor of claim 1; and a pharmaceutically acceptable carrier or excipient. 81-92. (canceled)
 93. The Hv1 inhibitor of claim 1, wherein the engineered polypeptide components are joined or linked together via a linker.
 94. The Hv1 inhibitor of claim 93, wherein the linker comprises a rigid or flexible linker.
 95. The Hv1 inhibitor of claim 93, wherein the linker comprises a rigid or flexible amino acid linker.
 96. The Hv1 inhibitor of claim 95, wherein the rigid or flexible amino acid linker is ten amino acids in length.
 97. The Hv1 inhibitor of claim 1, wherein the engineered polypeptide components are covalently joined or linked together.
 98. The Hv1 inhibitor of claim 29, wherein at least one of the two engineered polypeptide components consists of an amino acid sequence: (SEQ ID NO: 129) SSTCIPSGQPCADSDDCCETFHCKVVVFFTSKFMCRRVWGKD.


99. The Hv1 inhibitor of claim 98, wherein each of the two engineered polypeptide components consists of an amino acid sequence: (SEQ ID NO: 129) SSTCIPSGQPCADSDDCCETFHCKVVVFFTSKFMCRRVWGKD. 